Kuroda, Ken-ichi et al. published their research in Organic Geochemistry in 2006 | CAS: 3929-47-3

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Related Products of 3929-47-3

Analytical pyrolysis of lignin: products stemming from 灏?5 substructures was written by Kuroda, Ken-ichi;Nakagawa-Izumi, Akiko. And the article was included in Organic Geochemistry in 2006.Related Products of 3929-47-3 This article mentions the following:

Five phenolic 2-arylcoumarans containing a 灏?5 linkage: I (R = CH2OH, R’ = CH:CHCH2OH) (II), I (R = CH2OH, R’ = CH:CHCHO) (III), I (R = Me, R’ = CH:CHCH2OH) (IV), I (R = Me, R’ = CH:CHCHO) (V), I (R = Me, R’ = CH:CHMe) (VI), and diazomethane-methylated II (VII), were pyrolyzed at 500鎺?for 4 s. The products were analyzed by gas chromatog. and gas chromatog./mass spectrometry. The major products of II–V and VII were 4-methylguaiacol (VIII) and 1,2-dimethoxy-4-methylbenzene, resp., stemming from the A moiety of the 2-arylcoumarans. I–V having the ring B with a CH:CHCH2OH or CH:CHCHO side chain provided VIII in a larger yield than dehydrodiisoeugenol VI having the ring B with a CH=CHCH3 side chain; the yields of 4 were 閳?.6, 5.7-4.6, and 0.9 mol% from II, III–V and VI, resp. Characterization of the dimeric products of II showed the 浼?aryl ether opened-dimers with the hydrogenated C浼?C灏?bond being the precursors of VIII. Based on these results, guaiacyl and syringyl 灏?5 substructures were proposed as potential pyrolytic origins for VIII and 3,5-dimethoxy-4-methylphenol in anal. pyrolysis of soft- and hardwood lignins. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Related Products of 3929-47-3).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Related Products of 3929-47-3

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