Category: 38256-93-8

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Formula: C4H11NO.

Tassoti, Sebastian;Walenta, Martin;Poecheim, Alexander;Buchberger, Kathrin;Kunert, Olaf;Zangger, Klaus research published 《 Solvent-independent determination of heteroatom protonation states from NMR spectra by differential deuterium isotope shifts》, the research content is summarized as follows. The NMR-spectroscopy based structure elucidation of organic mols. containing heteroatoms is often obstructed by the difficulties in determining the heteroatom protonation states. Here we describe a simple but broadly applicable approach for the determination of the protonation states of heteroatoms. Differential deuterium isotope shifts observed upon the addition of small amounts of H₂O or D₂O to any solvent can be used to determine the protonation states of heteroatoms.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Formula: C4H11NO

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Recommanded Product: 2-Methoxy-N-methylethanamine.

Shao, Min;Chen, Xiaojuan;Yang, Fang;Song, Xiaojuan;Zhou, Yang;Lin, Qianmeng;Fu, Ying;Ortega, Raquel;Lin, Xiaojing;Tu, Zhengchao;Patterson, Adam V.;Smaill, Jeff B.;Chen, Yongheng;Lu, Xiaoyun research published 《 Design, Synthesis, and Biological Evaluation of Aminoindazole Derivatives as Highly Selective Covalent Inhibitors of Wild-Type and Gatekeeper Mutant FGFR4》, the research content is summarized as follows. A series of aminoindazole derivatives I [R¹ = 1-(2,6-dichloro-3-fluoro-phenyl)ethyl, 1-(2,6-dichlorophenyl)ethyl, (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, (3,5-dichloro-4-pyridyl)methyl, 1-(3,5-dichloro-4-pyridyl)propyl; R² = H, Me, Cl, etc.; R³ = H, MeO; R⁴ = H, 4-methylpiperazin-1-yl, morpholino, etc.] was designed and synthesized as new irreversible inhibitors of wild-type and gatekeeper mutant FGFR4. One representative compound I [R¹ = (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, R² = F, R³ = H, R⁴ = 4-morpholino-1-piperidyl] exhibited excellent potency against FGFR4, FGFR4^V550L and FGFR4^V550M with nanomolar activity in both the biochem. and cellular assays while sparing FGFR1/2/3. While compound I [R¹ = (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, R² = F, R³ = H, R⁴ = 4-morpholino-1-piperidyl] demonstrated modest in vivo antitumor efficacy in nude mice bearing the Huh-7 xenograft model consistent with its unfavorable pharmacokinetic properties, it provided a promising new starting point for future drug discovery combating FGFR4 gatekeeper mediated resistance in HCC patients.

Recommanded Product: 2-Methoxy-N-methylethanamine, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. HPLC of Formula: 38256-93-8.

Shekh-Ahmad, Tawfeeq;Bialer, Meir;Yavin, Eylon research published 《 Synthesis and anticonvulsant evaluation of dimethylethanolamine analogues of valproic acid and its tetramethylcyclopropyl analogue》, the research content is summarized as follows. Summary: Background: Valproic acid (VPA) is a major antiepileptic drug (AED) that is less potent than other AEDs. 2,2,3,3-Tetramethylcyclopropanecarboxylic acid (TMCA) is an inactive cyclopropyl analog of VPA that serves as a starting material for the synthesis of CNS-active compounds Methods: New conjugation products between N,N’-dimethylethanolamine to VPA and TMCA to form N,N-dimethylethanolamine valproate (DEVA) and N,N-dimethylethanolamine 2,2,3,3-tetramethylcyclopropionate were synthesized and their anticonvulsant activity was assessed in the maximal electroshock seizure (MES) and s.c. metrazol (scMet) seizure tests and the hippocampal kindling model in mice and/or rats. An amide analog of DEVA (DEVAMIDE) was also synthesized and evaluated. The pharmacokinetics of DEVA and DEVAMIDE was comparatively evaluated in rats. Results: In rats DEVA acted as a prodrug of VPA and had ED₅₀ values of 73 mg/kg and 158 mg/kg in the MES and the hippocampal kindling models, resp. At these two anticonvulsant models DEVA was seven-times more potent than VPA. DEVAMIDE was active in the MES test at doses of 100 mg/kg (mice) and its rat-MES-ED₅₀ = 38.6 mg/kg however, its protective index (PI = TD₅₀/ED₅₀) was twice lower than DEVA’s PI. The TMCA analogs were inactive at the mice MES and scMet models. DEVA underwent rapid metabolic hydrolysis to VPA and consequently, in its pharmacokinetic anal. only VPA plasma levels were monitored. In contrast, DEVAMIDE was stable in whole blood. Conclusion: DEVA acts in rats as a prodrug of VPA yet shows a more potent anticonvulsant activity than VPA. DEVAMIDE acted as the drug on its own and was more potent than DEVA at the rat-MES test.

HPLC of Formula: 38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. SDS of cas: 38256-93-8.

Siewert, Riko;Zherikova, Kseniya V.;Verevkin, Sergey P. research published 《 Non-Covalent Interactions in Molecular Systems: Thermodynamic Evaluation of the Hydrogen-Bond Strength in Amino-Ethers and Amino-Alcohols》, the research content is summarized as follows. The intramol. hydrogen bond (intra-HB) is one of the best-known examples of non-covalent interactions in mols. Among the different types of intramol. hydrogen bonding, the NH···O hydrogen bond in amino-alcs. and amino-ethers is one of the weakest. In contrast to the strong OH···N intramol. hydrogen bond, the strength of the NH···O bond can hardly be measured with conventional spectroscopic methods, even for simple amino-alcs., since the band belonging to the NH···O conformer merges with the free OH band. In this work, we developed a combination of G4 calculations, and a method based on exptl. vaporization enthalpies to determine the NH···O hydrogen bonding strength. The archetypal compounds for this study are 2-amino-1-ethanol and 3-amino-1-propanol as well as their resp. methoxy analogs. Based on these mols., different series were studied to investigate various factors influencing NH···O intra-HB strength. In the first series, the influence of alkylation near the hydroxy or methoxy group and the amino group in sterically hindered aminoalcs. was examined In the second series, the influence of alkylation of the amino-group was investigated. In the third series, the effect of extending the alkyl chain between functional groups was studied.

SDS of cas: 38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. COA of Formula: C4H11NO.

Savych, Olena;Kuchkovska, Yuliya O.;Bogolyubsky, Andrey V.;Konovets, Anzhelika I.;Gubina, Kateryna E.;Pipko, Sergey E.;Zhemera, Anton V.;Grishchenko, Alexander V.;Khomenko, Dmytro N.;Brovarets, Volodymyr S.;Doroschuk, Roman;Moroz, Yurii S.;Grygorenko, Oleksandr O. research published 《 One-Pot Parallel Synthesis of 5-(Dialkylamino)tetrazoles》, the research content is summarized as follows. Two protocols for the combinatorial synthesis of 5-(dialkylamino)tetrazoles were developed. The best success rate (67%) was shown by the method that used primary and secondary amines, 2,2,2-trifluoroethylthiocarbamate, and sodium azide as the starting reagents. The key steps included the formation of unsym. thiourea, subsequent alkylation with 1,3-propane sultone and cyclization with azide anion. A 559-member aminotetrazole library was synthesized by this approach; the overall readily accessible (REAL) chem. space covered by the method exceeded 7 million feasible compounds

COA of Formula: C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Application of C4H11NO.

Sawatzky, Ryan S.;Ferguson, Michael J.;Stradiotto, Mark research published 《 Thieme Chemistry Journals Awardees – Where Are They Now? Efficient Cross-Coupling of Secondary Amines/Azoles and Activated (Hetero)Aryl Chlorides Using an Air-Stable DPEPhos/Nickel Pre-Catalyst》, the research content is summarized as follows. Synthesis and characterization of the new air-stable pre-catalyst (DPEPhos)Ni(2-mesityl)Br (I) is reported, along with the application of this pre-catalyst in the cross-coupling of secondary amines/azoles with activated (hetero)aryl chlorides to afford tertiary (hetero)anilines. The performance of I in these cross-couplings is competitive with some of the best and/or most widely employed nickel catalysts for such transformations.

Application of C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. HPLC of Formula: 38256-93-8.

Remeur, Camille;Kelly, Christopher B.;Patel, Niki R.;Molander, Gary A. research published 《 Aminomethylation of Aryl Halides Using α-Silylamines Enabled by Ni/Photoredox Dual Catalysis》, the research content is summarized as follows. In the presence of the ruthenium photocatalyst [Ru(bipy)₃](PF₆^–)₂ and the nickel catalyst [Ni(dtbpy)(OH₂)₄]Cl₂ (dtbpy = 4,4′-di-tert-butyl-2,2′-bipyridine), aryl bromides and iodides such as 4-bromobenzonitrile underwent chemoselective aminomethylation reactions with aminomethylsilanes such as 1-(dimethylphenylsilylmethyl)piperidine in DMF under irradiation with blue LED for 24-36 h at ambient temperature to yield benzylic amines such as 4-(1-piperidinylmethyl)benzonitrile in 41-70% yields. The low oxidation potential of the silylmethyl amines enabled facile single electron transfer (SET) oxidation of the amine followed by rapid desilylation; the resultant α-amino radicals were competent to undergo nickel-mediated cross-coupling with aryl bromides and iodides.

HPLC of Formula: 38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Application In Synthesis of 38256-93-8.

Richard-Bildstein, Sylvia;Aissaoui, Hamed;Pothier, Julien;Schafer, Gabriel;Gnerre, Carmela;Lindenberg, Eleanor;Lehembre, Francois;Pouzol, Laetitia;Guerry, Philippe research published 《 Discovery of the Potent, Selective, Orally Available CXCR7 Antagonist ACT-1004-1239》, the research content is summarized as follows. The chemokine receptor CXCR7, also known as ACKR3, is a seven-transmembrane G-protein-coupled receptor (GPCR) involved in various pathologies such as neurol. diseases, autoimmune diseases, and cancers. By binding and scavenging the chemokines CXCL11 and CXCL12, CXCR7 regulates their extracellular levels. From an original high-throughput screening campaign emerged an arylketoamide hit among others. The hit-to-lead optimization led to the discovery of a novel chemotype series of acylaminopiperidinecarboxamides. This series provided CXCR7 antagonists that block CXCL11- and CXCL12-induced ss-arrestin recruitment. Further structural modifications on the acylaminopiperidinecarboxamide framework yielded compounds with high CXCR7 antagonistic activities and balanced ADMET properties. The effort described herein culminated in the discovery of ACT-1004-1239 I. Biol. characterization of I demonstrated that it is a potent, insurmountable antagonist. Oral administration of I in mice up to 100 mg/kg led to a dose-dependent increase of plasma CXCL12 concentration

Application In Synthesis of 38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Application of C4H11NO.

Rosca, Sorin-Claudiu;Roisnel, Thierry;Dorcet, Vincent;Carpentier, Jean-Francois;Sarazin, Yann research published 《 Potassium and Well-Defined Neutral and Cationic Calcium Fluoroalkoxide Complexes: Structural Features and Reactivity》, the research content is summarized as follows. The fluorinated aminoether alcs. (1-aza-12-crown-4)CH₂C(CF₃)₂OH ({RO₁^F}H), (MeOCH₂CH₂)₂NCH₂C(CF₃)₂OH ({RO₂^F}H), and (MeOCH₂CH₂)(Me)NCH₂C(CF₃)₂OH ({RO₃^F}H) have been synthesized and used to prepare the heteroleptic calcium amido complexes {RO_x^F}Ca(N(SiMe₂R)₂) (4–7; x = 2, 3, R = H, Me). The ability to form stable complexes varies with the chelating and electron-donating ability of the aminoether alkoxide ligand, as exemplified by the authors’ failure to isolate cleanly the elusive {RO₁^F}Ca(N(SiMe₂R)₂). X-ray diffraction studies show that, in the solid state, intramol. Ca···F interactions help reach coordinative saturation in the dimeric [{RO₂^F}Ca(N(SiMe₃)₂)]₂ ([4]₂), [{RO₂^F}Ca(N(SiMe₂H)₂)]₂ ([5]₂), [{RO₃^F}Ca(N(SiMe₃)₂)]₂ ([6]₂), and [{RO₃^F}Ca(N(SiMe₂H)₂)]₂ ([7]₂), which crystallized free of solvent coligands. Similar stabilizing K···F patterns were found in the polymetallic potassium fluoroalkoxides [{RO₁^F}K]₂ ([1]₂), [{RO₂^F}K]₄ ([2]₄), and [{RO₃^F}K]₄ ([3]₄); [2]₄ and [3]₄ form heterocubanes in the solid state. Examination of the XRD data for [1]₂-[7]₂ shows that metal···F interactions can be favored over binding of O_ether atoms for calcium and potassium. Pulse-gradient spin-echo NMR spectroscopy shows that the complexes remain aggregated in aromatic solvents. The solvent-free salts [{RO_x^F}Ca⁺]·[H₂N{B(C₆F₅)₃}₂^–] (x = 1 (8), 2 (9), 3 (10)) were obtained by treating 4–7 with [H(OEt₂)₂⁺]·[H₂N{B(C₆F₅)₃}₂^–] or by reacting Ca(N(SiMe₃)₂)₂ with [{RO_x^F}HH⁺]·[H₂N{B(C₆F₅)₃}₂^–]; the solid-state structures of [8·H₂O]₂ and [9·H₂O]₂ again showed Ca···F contacts. Complexes 5–7 are promising catalysts for the regiospecific anti-Markovnikov hydrophosphination of styrene with diphenylphosphine, affording TOF values as high as 52 mol_subst mol_Ca^-1 h^-1 with up to 400 equiv of substrates within 1-2 h at 60°.

Application of C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Name: 2-Methoxy-N-methylethanamine.

Pinaud, Marine;Le Gall, Erwan;Presset, Marc research published 《 Mixed Aliphatic Organozinc Reagents as Nonstabilized C_sp³-Nucleophiles in the Multicomponent Mannich Reaction》, the research content is summarized as follows. The use of mixed aliphatic organozinc reagents in the multicomponent Mannich reaction was described. A large variety of primary, secondary and tertiary organozinc reagents, secondary amines and aromatic or aliphatic aldehydes could be used for the straightforward preparation of densely substituted amines. The three-component reaction could addnl. be performed starting from alkyl halides under reductive (Barbier-type) conditions.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Name: 2-Methoxy-N-methylethanamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem