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Benzoic acid, 3-bromo-4,5-dihydroxy-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65841-10-3

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65841-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65841-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65841-10:
(7*6)+(6*5)+(5*8)+(4*4)+(3*1)+(2*1)+(1*0)=133
133 % 10 = 3
So 65841-10-3 is a valid CAS Registry Number.

65841-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-bromo-4,5-dihydroxybenzoate

1.2 Other means of identification

Product number -
Other names 3-bromo-4,5-dihydroxy-benzoic acid methyl ester

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:65841-10-3 SDS

65841-10-3Relevant academic research and scientific papers

METHOD FOR PREPARING DIPHENYLMETHANE DERIVATIVES

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Paragraph 0247; 0248, (2017/09/29)

The present invention relates to an improved process for preparing a diphenyl methane derivative which is useful as an inhibitor of a sodium-dependent glucose transporter (SGLT). Since the process of the present invention is performed by convergent synthe

The biosynthesis of ubiquinone: Synthesis and enzymatic modification of biosynthetic precursors

Shepherd, Jennifer A.,Poon, Wayne W.,Myles, David C.,Clarke, Catherine F.

, p. 2395 - 2398 (2007/10/03)

The synthesis of key intermediates in the eukaryotic biosynthetic pathway of ubiquinone (Q) and the biotransformation of these materials with yeast (S.cerevisiae) mitochondria are described. The synthesis of Q aromatic precursors 2, 3, and 4 (n = 3 in all cases) relies on the palladium (0) catalyzed coupling of farnesyl tributylstannane with suitably functionalized aryl halides. Preliminary experiments show that incubation of synthetic substrate 3 with mitochondria from yeast containing the 3,4-dihydroxy-5-hexaprenylbenzoate methyltransferase gene (COQ3) and S-[methyl-3H]adenosyl-L-methionine yields radiolabeled 4.

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