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Benzoic acid, 3-[(3-carboxy-1-oxopropyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

259222-20-3

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259222-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259222-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,2,2 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 259222-20:
(8*2)+(7*5)+(6*9)+(5*2)+(4*2)+(3*2)+(2*2)+(1*0)=133
133 % 10 = 3
So 259222-20-3 is a valid CAS Registry Number.

259222-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-carboxypropanoylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names Succinanilsaeure-carbonsaeure-(3)

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:259222-20-3 SDS

259222-20-3Downstream Products

259222-20-3Relevant academic research and scientific papers

Towards small molecule inhibitors of mono-ADP-ribosyltransferases

Ekblad, Torun,Lindgren, Anders E.G.,Andersson, C. David,Caraballo, Rémi,Thorsell, Ann-Gerd,Karlberg, Tobias,Spjut, Sara,Linusson, Anna,Schüler, Herwig,Elofsson, Mikael

supporting information, p. 546 - 551 (2015/04/14)

Protein ADP-ribosylation is a post-translational modification involved in DNA repair, protein degradation, transcription regulation, and epigenetic events. Intracellular ADP-ribosylation is catalyzed predominantly by ADP-ribosyltransferases with diphtheri

Synthesis, anticholinesterase activity and structure-activity relationships of m-Aminobenzoic acid derivatives

Trujillo-Ferrara, Jose,Montoya Cano, Leticia,Espinoza-Fonseca, Michel

, p. 1825 - 1827 (2007/10/03)

The synthesis, acetylcholinesterase inhibitory capacity and structure-activity relationships of simple-structured m-Aminobenzoic acid derivatives are reported. Compound 1b was found to be more potent than galanthamine and tacrine in inhibiting acetylcholinesterase.

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