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148547-19-7

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148547-19-7 Usage

Chemical Properties

Colorless low melting solid

Uses

Methyl 4-bromo-3-methylbenzoate may be used in the preparation of:4-bromo-3-vinylbenzoic acid4-bromo-3-(methylphenyl)methanolmethyl (E)-4-bromo-3-[(phenylmethoxyimino)methyl]benzoateIt may be used as a starting material in the total synthesis of (-)-martinellic acid.

General Description

Methyl 4-bromo-3-methylbenzoate, an aromatic ester, undergoes Suzuki coupling with 2-chloroboronic acid to afford the corresponding biaryl.

Check Digit Verification of cas no

The CAS Registry Mumber 148547-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,5,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148547-19:
(8*1)+(7*4)+(6*8)+(5*5)+(4*4)+(3*7)+(2*1)+(1*9)=157
157 % 10 = 7
So 148547-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO2/c1-6-5-7(9(11)12-2)3-4-8(6)10/h3-5H,1-2H3

148547-19-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A19078)  Methyl 4-bromo-3-methylbenzoate, 97%   

  • 148547-19-7

  • 1g

  • 179.0CNY

  • Detail
  • Alfa Aesar

  • (A19078)  Methyl 4-bromo-3-methylbenzoate, 97%   

  • 148547-19-7

  • 5g

  • 536.0CNY

  • Detail
  • Alfa Aesar

  • (A19078)  Methyl 4-bromo-3-methylbenzoate, 97%   

  • 148547-19-7

  • 25g

  • 1509.0CNY

  • Detail

148547-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-bromo-3-methylbenzoate

1.2 Other means of identification

Product number -
Other names methyl 3-methyl-4-bromobenzoate

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:148547-19-7 SDS

148547-19-7Relevant articles and documents

Electro-Oxidative Selective Esterification of Methylarenes and Benzaldehydes

Yu, Congjun,?zkaya, Bünyamin,Patureau, Frederic W.

supporting information, p. 3682 - 3687 (2021/02/01)

A mild and green electro-oxidative protocol to construct aromatic esters from methylarenes and alcohols is herein reported. Importantly, the reaction is free of metals, chemical oxidants, bases, acids, and operates at room temperature. Moreover, the design of the electrolyte was found critical for the oxidation state and structure of the coupling products, a rarely documented effect. This electro-oxidative coupling process also displays exceptional tolerance of many fragile easily oxidized functional groups such as hydroxy, aldehyde, olefin, alkyne, as well as neighboring benzylic positions. The enantiomeric enrichment of some chiral alcohols is moreover preserved during this electro-oxidative coupling reaction, making it overall a promising synthetic tool.

Hydrogen sulfide induced supramolecular self-assembly in living cells

Wei, Simin,Zhou, Xi-Rui,Huang, Zhentao,Yao, Qingxin,Gao, Yuan

supporting information, p. 9051 - 9054 (2018/08/21)

Here we developed a critical gasotransmitter (H2S) mediated reduction to induce supramolecular self-assembly in multiple living cell lines. Specifically, the reduction converted an azido group to an amine which allowed the formation of intramolecular hydrogen bonds. The hydrogen bonds planarized the assembling molecules and promoted the supramolecular self-assembly.

BORON-CONTAINING SMALL MOLECULES

-

Paragraph 0189, (2013/06/04)

This invention provides novel compounds, methods of using the compounds, and pharmaceutical formulations comprising the compounds.

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