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189351-15-3

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189351-15-3 Usage

Description

Corchoiol C is a natural triterpenoid compound derived from the cork of the Quercus suber tree, exhibiting a range of biological activities such as antimicrobial, antioxidant, and anti-inflammatory properties. Its unique chemical structure and diverse bioactivities position it as a promising candidate for research and potential therapeutic applications in various diseases and conditions.

Uses

Used in Pharmaceutical Industry:
Corchoiol C is used as a therapeutic agent for its potential role in the treatment of various diseases and conditions, including cancer, neurodegenerative disorders, and skin diseases, due to its antimicrobial, antioxidant, and anti-inflammatory properties.
Used in Cosmetics Industry:
Corchoiol C is used as an active ingredient in skincare products for its antioxidant and anti-inflammatory properties, which can help protect the skin from environmental damage and reduce inflammation.
Used in Food Industry:
Corchoiol C is used as a natural preservative and antioxidant in food products to extend shelf life and maintain the quality of the food by preventing oxidation and microbial growth.
Used in Agricultural Industry:
Corchoiol C is used as a biopesticide to protect crops from microbial and fungal infections, reducing the need for chemical pesticides and promoting sustainable agriculture.
Used in Nutraceutical Industry:
Corchoiol C is used as a dietary supplement to promote overall health and well-being by providing antioxidant and anti-inflammatory benefits, as well as supporting the immune system.

Check Digit Verification of cas no

The CAS Registry Mumber 189351-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,3,5 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 189351-15:
(8*1)+(7*8)+(6*9)+(5*3)+(4*5)+(3*1)+(2*1)+(1*5)=163
163 % 10 = 3
So 189351-15-3 is a valid CAS Registry Number.

189351-15-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-4-Hydroxy-4-[(1E,3S)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethyl -2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names corchoionol C

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:189351-15-3 SDS

189351-15-3Relevant articles and documents

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

Calis, Ihsan,Kuruuezuem-Uz, Ayse,Lorenzetto, Piergiorgio A,Rueedi, Peter

, p. 451 - 457 (2002)

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

Yamano, Yumiko,Ito, Masayoshi

, p. 541 - 546 (2007/10/03)

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.

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