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90332-29-9

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90332-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90332-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90332-29:
(7*9)+(6*0)+(5*3)+(4*3)+(3*2)+(2*2)+(1*9)=109
109 % 10 = 9
So 90332-29-9 is a valid CAS Registry Number.

90332-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-(4-methoxyphenyl)ethyl]benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 3,5-dihydroxy-4'-methoxybibenzyl

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:90332-29-9 SDS

90332-29-9Relevant articles and documents

Resveratrol Derivatives and Their Role as Potassium Channels Modulators

Orsini,Verotta,Lecchi,Restano,Curia,Redaelli,Wanke

, p. 421 - 426 (2007/10/03)

A series of stilbenoid analogues of resveratrol (trans-3,4′ ,5-trihydroxystilbene) with a stilbenic or a bibenzylic skeleton have been prepared by partial synthesis from resveratrol and dihydroresveratrol. The synthesized compounds have been evaluated for their ability to modulate voltage-gated channels.

Synthesis of biologically active polyphenolic glycosides (combretastatin and resveratrol series)

Orsini, Fulvia,Pelizzoni, Francesca,Bellini, Barbara,Miglierini, Giuliana

, p. 95 - 109 (2007/10/03)

(E)-3-(β-D-Glucopyranosyloxy)-4',5-dihydroxystilbene (resveratrol 3-β-D-glucoside, piceid), (Z)-2',3'-dihydroxy-3,4,4',5-tetramethoxystilbene (combretastatin A-1), (Z)-3'-hydroxy-3,4,4', 5-tetramethoxystilbene (combretastatin A-4), (Z)-2'-hydroxy-3,4,4',5-tetramethoxystilbene (combretastatin iso-A-4), α,β-dihydro-2',3'-dihydroxy-3,4,4',5-tetramethoxystilbene (combretastatin B-1), the corresponding glucosides, and related compounds have been synthesized via Wittig reactions followed by,glucosylation under phase-transfer catalysis. Most of the compounds synthesized have been tested with respect to biological activity (cytostatic, cytotoxic, antimitotic, neurotoxic, antiplatelet aggregation activity).

Spasmolytic Principle from Rheum webbianum Royle

Chaudhar, M.,Jain, G. K.,Sarin, J. P.,Khanna, N. M.

, p. 1163 - 1164 (2007/10/02)

The structure of spasmolytic principle, isolated from Rheum webbianum, has ben established as 3',5'-dihydroxy-4-methoxystilbene on the basis of physico-chemical studies.

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