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5-ACETAMIDO-2-BROMOBENZOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22921-67-1

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22921-67-1 Usage

Chemical Properties

Lilac-greyish powder

Check Digit Verification of cas no

The CAS Registry Mumber 22921-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,2 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22921-67:
(7*2)+(6*2)+(5*9)+(4*2)+(3*1)+(2*6)+(1*7)=101
101 % 10 = 1
So 22921-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrNO3/c1-5(12)11-6-2-3-8(10)7(4-6)9(13)14/h2-4H,1H3,(H,11,12)(H,13,14)/p-1

22921-67-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L09626)  5-Acetamido-2-bromobenzoic acid hydrate, 95%   

  • 22921-67-1

  • 5g

  • 709.0CNY

  • Detail

  • Alfa Aesar

  • (L09626)  5-Acetamido-2-bromobenzoic acid hydrate, 95%   

  • 22921-67-1

  • 25g

  • 2732.0CNY

  • Detail

22921-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ACETAMIDO-2-BROMOBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 5-Acetylamino-2-brom-benzoesaeure

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:22921-67-1 SDS

22921-67-1Relevant academic research and scientific papers

3-HYDROXY-6H-BENZO [C] CHROMENE-6-ONE DERIVATIVE AND MANUFACTURING METHOD THEREOF

-

Paragraph 0155, (2013/12/03)

A method of manufacturing a compound or a salt thereof expressed with a formula (III) below, characterized by causing a compound or a salt thereof expressed with a formula (I) below and a compound or a salt thereof expressed with a formula (II) below to r

Supramolecular control of selectivity in hydroformylation of vinyl arenes: Easy access to valuable β-aldehyde intermediates

Dydio, Pawel,Reek, Joost N. H.

supporting information, p. 3878 - 3882 (2013/05/09)

Go against the flow! A rationally designed regioselective hydroformylation catalyst, [Rh/L], in which noncovalent ligand-substrate interactions allow the unprecedented reversal of selectivity from the typical α-aldehyde to the otherwise unfavored product β-aldehyde, is reported. This catalytic system opens up novel and sustainable synthetic pathways to important intermediates for the fine-chemicals industry.

Heterocyclic compounds useful as inhibitors of tyrosine kinases

-

, (2008/06/13)

Disclosed are novel compounds of formula (I): wherein Ar1, Ra, R4, R5, X and Y are defined below, which are useful as inhibitors of certain protein tyrosine kinases and are thus useful for treating diseases asso

Heterocyclic compounds useful as inhibitors of tyrosine kinases

-

, (2008/06/13)

Disclosed are novel compounds of formula (I): wherein Ar1, Ra, R4, R5, X and Y are defined below, which are useful as inhibitors of certain protein tyrosine kinases and are thus useful for treating diseases asso

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