189351-15-3

Basic information

• Product Name: Corchoiol C
• Synonyms: Corchoiol C;Corchoionol C;Corchoionoside C aglycon
• CAS NO: 189351-15-3
• Molecular Formula: C₁₃H₂₀O₃
• Molecular Weight: 224.2961
• Mol File: 189351-15-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Corchoiol C(CAS DataBase Reference)
• NIST Chemistry Reference: Corchoiol C(189351-15-3)
• EPA Substance Registry System: Corchoiol C(189351-15-3)

Safety Data

• Hazardous Substances Data: 189351-15-3(Hazardous Substances Data)

Usage

General Description

Corchoiol C is a natural compound that belongs to the class of triterpenoids. It is derived from the cork of the Quercus suber tree and has been found to possess various biological activities, including antimicrobial, antioxidant, and anti-inflammatory properties. Corchoiol C has been studied for its potential use in the treatment of various diseases and conditions, such as cancer, neurodegenerative disorders, and skin diseases. Its unique chemical structure and diverse bioactivities make it a promising candidate for further research and potential therapeutic applications.

Upstream product

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• 863032-44-4 Acetic acid (E)-(S)-3-[(1S,4S,6R)-4-(tert-butyl-dimethyl-silanyloxy)-2,2,6-trimethyl-7-oxa-bicyclo[4.1.0]hept-1-yl]-1-methyl-allyl ester 
• 863032-42-2 Acetic acid (E)-(S)-3-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-1-methyl-allyl ester 
• 863032-51-3 (E)-(S)-4-[(R)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-ol 
• 863032-43-3 Vomifoliol-monoacetat 
• 54835-70-0 corchoionoside C 
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Downstream Products

• 863032-48-8 2,2-Dimethyl-propionic acid (2R,3R,4S,5R,6R)-4,5-bis-(2,2-dimethyl-propionyloxy)-6-(2,2-dimethyl-propionyloxymethyl)-2-[(E)-(S)-3-((S)-1-hydroxy-2,6,6-trimethyl-4-oxo-cyclohex-2-enyl)-1-methyl-allyloxy]-tetrahydro-pyran-3-yl ester 
• 54835-70-0 corchoionoside C 

Relevant articles and documents

(6S)-Hydroxy-3-oxo-alpha-ionol glucosides from Capparis spinosa fruits.

Two new (6S)-hydroxy-3-oxo-alpha-ionol glucosides, together with corchoionoside C ((6S,9S)-roseoside) and a prenyl glucoside, were isolated from mature fruits of Capparis spinosa. The structures were established on the basis of spectroscopic, chiroptic and chemical evidence. In addition, the 13C-resonance of C-9 was found to be of particular diagnostic value in assigning the absolute configuration at that center in ionol glycosides. The alpha-ionol derivatives are metabolites of (+)-(S)-abscisic acid.

Synthesis of optically active vomifoliol and roseoside stereoisomers

A synthesis of optically active vomifoliol stereoisomers 1-4 and their glucosides, roseoside stereoisomers 5-8, was accomplished via α-acetylenic alcohol 11a or 11b effectively prepared by an asymmetric transfer hydrogenation of α,β-acetylenic ketone 10. Simultaneous separation of these stereoisomers by HPLC was also perfomed.