Horinishi, Asako et al. published their research in ACS Food Science & Technology in 2022 | CAS: 29106-49-8

(2R,2’R,3R,3’R,4R)-2,2′-Bis(3,4-dihydroxyphenyl)-[4,8′-bichromane]-3,3′,5,5′,7,7′-hexaol (cas: 29106-49-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Related Products of 29106-49-8

Changes in Proanthocyanidin Content during the Processing of Umeshu, a Spirit-Based Liqueur of Japanese Apricot (Prunus mume Sieb. et Zucc.) Fruit was written by Horinishi, Asako;Toyama, Yoshimasa;Watanabe, Minoru;Ayano, Shigeru;Ozaki, Yoshihiko. And the article was included in ACS Food Science & Technology in 2022.Related Products of 29106-49-8 The following contents are mentioned in the article:

Japanese apricot (Prunus mume Sieb. et.Zucc.), also known as Ume, is used as a food item and a folk remedy in most east Asian countries, including Japan. Umeshu is a liqueur made from Ume and is one of the most popular products obtained from this fruit. The polyphenols (PPs) and proanthocyanidins (PAs) present in Umeshu and the residual fruit obtained post immersion were analyzed. We are the first to report the characteristics of the phenolic compounds obtained during the processing of Umeshu. The concentration of PA in Umeshu was approx. 16μg/mL, and this concentration was significantly lower than the concentrations of PA present in other liqueurs. It is believed that most of the PAs contained in Umeshu leach out from the endocarp. The total amounts of extractable PAs decreased, and the total amounts of nonextractable PAs increased in Umeshu and the residual fruit during the processing stage. This study involved multiple reactions and reactants, such as (2R,2’R,3R,3’R,4R)-2,2′-Bis(3,4-dihydroxyphenyl)-[4,8′-bichromane]-3,3′,5,5′,7,7′-hexaol (cas: 29106-49-8Related Products of 29106-49-8).

(2R,2’R,3R,3’R,4R)-2,2′-Bis(3,4-dihydroxyphenyl)-[4,8′-bichromane]-3,3′,5,5′,7,7′-hexaol (cas: 29106-49-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Related Products of 29106-49-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts