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2H-1-Benzopyran-4-ol, 7-bromo-3,4-dihydro-3-(phenylmethyl)-, (3S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204981-45-3

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204981-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204981-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,9,8 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 204981-45:
(8*2)+(7*0)+(6*4)+(5*9)+(4*8)+(3*1)+(2*4)+(1*5)=133
133 % 10 = 3
So 204981-45-3 is a valid CAS Registry Number.

204981-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-7-bromo-3-benzyl-4-chromanol

1.2 Other means of identification

Product number -
Other names (3 S ,4 R)-3-Benzyl-7-bromo-3,4-dihydro-benzopyran-4-ol

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:204981-45-3 SDS

204981-45-3Upstream product

204981-45-3Relevant academic research and scientific papers

Intermediates and processes for preparing substituted chromanol derivatives

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, (2008/06/13)

The invention relates to processes for preparing a compound of the formula and the enantiomer of said compound, wherein the benzoic acid moiety is attached at position 6 or 7 of the chroman ring, and R1, R2, and R3 are as

Benzoic acid substituted benzopyrans for the treatment of atherosclerosis

-

, (2008/06/13)

A method of treating atherosclerosis in a mammal, including a human, comprising administering to said mammal an amount of the compound of the formula an enantiomer, or the pharmaceutically acceptable salt thereof; effective to treat atherosclerosis, where

Processes for preparing substituted chromanol derivatives

-

, (2008/06/13)

PCT No. PCT/IB97/01024 Sec. 371 Date Mar. 5, 1999 Sec. 102(e) Date Mar. 5, 1999 PCT Filed Aug. 25, 1997 PCT Pub. No. WO98/11085 PCT Pub. Date Mar. 19, 1998The invention relates to processes for preparing a compound of the formula (X) and the enantiomer of

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