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220844-83-7

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220844-83-7 Usage

General Description

3-bromo-4-(dimethylamino)benzoic acid is a chemical compound with the molecular formula C10H11BrNO2. It is a derivative of benzoic acid that has a bromine atom at the 3-position and a dimethylamino group at the 4-position. 3-bromo-4-(dimethylamino)benzoic acid is mainly used as a building block in organic synthesis and pharmaceutical research, where it can be utilized in the creation of various pharmaceuticals and agrochemicals. It has potential applications in the development of drugs for various diseases and conditions, as well as in the production of crop protection agents. Additionally, 3-bromo-4-(dimethylamino)benzoic acid has been studied for its potential use in the synthesis of fluorescent dyes and as a precursor for the creation of advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 220844-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220844-83:
(8*2)+(7*2)+(6*0)+(5*8)+(4*4)+(3*4)+(2*8)+(1*3)=117
117 % 10 = 7
So 220844-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10BrNO2/c1-11(2)8-4-3-6(9(12)13)5-7(8)10/h3-5H,1-2H3,(H,12,13)

220844-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-4-(dimethylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names 3-bromanyl-4-(dimethylamino)benzoic acid

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:220844-83-7 SDS

220844-83-7Downstream Products

220844-83-7Relevant articles and documents

Catalyst and Additive-Free Direct Amidation/Halogenation of Tertiary Arylamines with N-haloimide/amides

Xu, Xiu-Juan,Amuti, Adila,Wusiman, Abudureheman

supporting information, p. 5002 - 5008 (2020/10/06)

An approach has been developed for the amidation (halogenation) of tertiary arylamines by electrophilic activation using N-haloimide/amides. Several control experiments have been performed, and the coupling reaction outcomes indicated that the N-haloimide/amide brings three major functions, including electrophilic activation, aromatic halogenation and nucleophilic nitrogen sources. This cascade reaction features simple manipulation, requires no additional catalyst, oxidant or additives, and is performed under mild conditions. (Figure presented.).

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