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629643-26-1

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629643-26-1 Usage

General Description

Gnetucleistol D is a natural product isolated from the roots of Gnetum cleistostachyum, a tropical climbing plant. It is a fatty acid ester derivative and belongs to the clerodane diterpenoids class of compounds. Gnetucleistol D has been found to possess anti-HIV activity by inhibiting the enzyme reverse transcriptase and has shown potential as a therapeutic agent for the treatment of HIV/AIDS. Its unique chemical structure and biological activity make it a promising candidate for further research and development in the field of antiretroviral drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 629643-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,9,6,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 629643-26:
(8*6)+(7*2)+(6*9)+(5*6)+(4*4)+(3*3)+(2*2)+(1*6)=181
181 % 10 = 1
So 629643-26-1 is a valid CAS Registry Number.

629643-26-1SDS

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 5-[2-(4-hydroxy-2-methoxyphenyl)ethenyl]benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Benzenediol,5-[(1E)-2-(4-hydroxy-2-methoxyphenyl)ethenyl]

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:629643-26-1 SDS

629643-26-1Downstream Products

629643-26-1Relevant articles and documents

Regioselective Biomimetic Synthesis of Dimeric Oxyresveratrol Derivatives

Ran, Lu,Li, Hongpeng,Chao, Ge,Kang, Xiaodong,Lei, Tian,Li, Wenling

supporting information, p. 1809 - 1812 (2020/09/18)

Oxyresveratrol and its methylated derivative as coupling precursors were efficiently prepared in four steps, with Wittig reactions and subsequent isomerization reactions as the key steps. The coupling reactions of oxyresveratrol under various oxidative conditions gave a complex and inseparable mixture of coupling products. The oxidative dimerizations of methylated oxyresveratrols catalyzed by horseradish peroxidase-H 2O 2or FeCl 3·6H 2O in an acetone system predominantly produced the 8-5-coupled and 8-10-coupled dihydrobenzofuran-type dimers, respectively. This regioselective biomimetic strategy might be useful in synthesizing other dimeric oxyresveratrol derivatives.

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