Kisanthia, Rattikon et al. published their research in ACS Sustainable Chemistry & Engineering in 2022 | CAS: 33171-05-0

Bisdemethoxycurcumin (cas: 33171-05-0) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.COA of Formula: C19H16O4

Impact of Conventional and Sustainable Solvents on the Yield, Selectivity, and Recovery of Curcuminoids from Turmeric was written by Kisanthia, Rattikon;Hunt, Andrew J.;Sherwood, James;Somsakeesit, La-or;Phaosiri, Chanokbhorn. And the article was included in ACS Sustainable Chemistry & Engineering in 2022.COA of Formula: C19H16O4 The following contents are mentioned in the article:

Extraction of pharmaceutically important curcuminoid platform mols. has been achieved from turmeric with ultrasound-assisted greener solvent extraction, demonstrating excellent performance and product recovery. Extraction of curcuminoids from turmeric was undertaken with both conventional and potentially bio-based solvents. Sustainable solvents, namely, Et acetate, ethanol, Cyrene, and deep eutectic solvent (DES-B5, 1:6 ChCl:1,4-butanediol) demonstrated high extraction yields of curcuminoids, including 24.36 ± 3.10, 25.30 ± 4.58, 23.51 ± 2.56, and 27.40 ± 3.80 mg/g of curcumin, resp. In contrast, curcumin extracted in lower polarity solvents such as hexane, toluene, and tetramethyloxolane was low at less than 7.0 mg/g, whereas 2-MeTHF, DMF, and THF represented moderate extraction yields of 13.80 ± 3.90, 14.43 ± 4.46, and 15.17 ± 2.08 mg/g, resp. DES-B5 with 10% water extracted the greatest yield of curcumin (46.70 ± 0.55 mg/g), bisdemethoxycurcumin (46.14 ± 0.82 mg/g), and demethoxycurcumin (10.63 ± 0.35 mg/g), followed by a simple and low energy product recovery method through the addition of water and precipitation COSMOtherm calculations suggested that the extraction efficiency was related to solvent interactions with the cell walls of the biomass, rather than the solubility of the curcuminoids. In addition, the application of ultrasound in extraction in combination with DES-B5 enabled the strong destruction of the plant matrix that was confirmed by SEM. The sustainability, efficiency, and toxicity of the proposed extraction methodologies were evaluated through the CHEM21 green metrics toolkit. The methods utilizing ethanol, Et acetate, and Cyrene in this work demonstrate a significant improvement over those previously published by 3-10 times of process mass intensity total, and DES-B5 also performed well under the green metrics assessment. Because of its high yields, low toxicity, being a bio-based solvent, inexpensive, and readily available, DES-B5 with 10% water is recommended as the greenest solvent for curcuminoid extraction under ultrasonication. This study involved multiple reactions and reactants, such as Bisdemethoxycurcumin (cas: 33171-05-0COA of Formula: C19H16O4).

Bisdemethoxycurcumin (cas: 33171-05-0) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.COA of Formula: C19H16O4

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