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Corchoroside is a naturally occurring chemical compound found in the bark of the cork oak tree (Quercus suber). It belongs to the class of triterpenoid saponins, which are known for their diverse biological activities. Corchoroside has been studied for its potential anti-inflammatory, anti-viral, and anti-cancer properties. Research suggests that it may modulate immune responses and exhibit cytotoxic effects on certain cancer cell lines. However, further studies are needed to fully understand its mechanisms of action and potential therapeutic applications.

508-76-9

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508-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 508-76-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 508-76:
(5*5)+(4*0)+(3*8)+(2*7)+(1*6)=69
69 % 10 = 9
So 508-76-9 is a valid CAS Registry Number.

508-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name corchoroside A

1.2 Other means of identification

Product number -
Other names 3β-(β-D-xylo-2,6-dideoxy-hexopyranosyloxy)-5,14-dihydroxy-19-oxo-5β,14β-card-20(22)-enolide

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:508-76-9 SDS

508-76-9Upstream product

508-76-9Downstream Products

508-76-9Relevant academic research and scientific papers

13C-NMR SPECTRA OF STROPHANTIDIN GLYCOSIDES OF Corchorus capsularis L.; STRUCTURE OF A NEW GLYCOSIDE: GLUCO(1-->6)OLITORISIDE

Ricca, Giuliana Severini,Casagrande, Cesare

, p. 349 - 352 (2007/10/02)

13C-NMR spectroscopy has been used to determine the structure of a new glycoside isolated from the seeds of Corchorus capsularis L.By spectral comparison of 13C-chemical shifts of the corresponding genin, monoside and bioside, we established that the glycoside is a trioside containing one boivinose and two glucose units; these were shown to be 1-->6β linked as in gentiobiose.This structure was confirmed by the chemical degradation of the glycoside chain, which afforded octa-O-acetyl-α-gentiobiose.

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