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164513-41-1

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164513-41-1 Usage

General Description

2-Bromo-5-(dimethylamino)benzoic acid methyl ester is a chemical compound with the molecular formula C10H12BrNO2. It is a methyl ester derivative of 2-bromo-5-(dimethylamino)benzoic acid, and it is commonly used as a building block in organic synthesis. 2-broMo-5-(diMethylaMino)benzoic acid Methyl ester is a yellow to brown solid with a melting point of around 137-139°C. It is often used in the pharmaceutical industry as an intermediate in the synthesis of various organic compounds, and it has potential applications in the field of medicinal chemistry. Additionally, it is important to handle and store this chemical with proper safety precautions, as it may be harmful if ingested, inhaled, or absorbed through the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 164513-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,5,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 164513-41:
(8*1)+(7*6)+(6*4)+(5*5)+(4*1)+(3*3)+(2*4)+(1*1)=121
121 % 10 = 1
So 164513-41-1 is a valid CAS Registry Number.

164513-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-5-dimethylamino-benzoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 2-bromo-5-(dimethylamino)benzoate

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:164513-41-1 SDS

164513-41-1Relevant articles and documents

Synthesis of Halogenated Anilines by Treatment of N, N-Dialkylaniline N-Oxides with Thionyl Halides

Reed, Hayley,Paul, Tyler R.,Chain, William J.

, p. 11359 - 11368 (2018/08/06)

The special reactivity of N,N-dialkylaniline N-oxides allows practical and convenient access to electron-rich aryl halides. A complementary pair of reaction protocols allow for the selective para-bromination or ortho-chlorination of N,N-dialkylanilines in up to 69% isolated yield. The generation of a diverse array of halogenated anilines is made possible by a temporary oxidation level increase of N,N-dialkylanilines to the corresponding N,N-dialkylaniline N-oxides and the excision of the resultant weak N-O bond via treatment with thionyl bromide or thionyl chloride at low temperature.

2-ARYL- AND 2-HETEROARYLTHIAZOLYL COMPOUNDS, METHODS FOR THEIR PREPARATION AND USE THEREOF

-

Page/Page column 41, (2009/10/22)

The present invention discloses fused heterobicyclic 2-aryl- and 2-heteroarylthiazolyl compounds and their pharmaceutically acceptable salts and esters thereof, which are useful for inhibiting the growth of cancerous cells, inhibiting human breast carcino

Synthesis and photochromic properties of 2H,9H-indeno[1,2-f]- and 3H,7H-indeno[2,1-i]-naphtho[2,1-b]pyrans

Gabbutt, Christopher D.,Heron, B. Mark,Mars, Craig A.,Partington, Steven M.

, p. 167 - 172 (2007/10/03)

Expedient syntheses of the 3-hydroxy- and 6-hydroxy- derivatives of 11H-benzo[a]-fluoren-11-one, obtained via Suzuki-Miyaura couplings are described. Reactions of these phenols with 1,1-diarylprop-2-yn-1-ols give indeno[2,1-i]- and indeno[1,2-f]-naphtho[2

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