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3-AMINO-N-3-PYRIDINYLBENZAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25844-48-8

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25844-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25844-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,4 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25844-48:
(7*2)+(6*5)+(5*8)+(4*4)+(3*4)+(2*4)+(1*8)=128
128 % 10 = 8
So 25844-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3O/c13-10-4-1-3-9(7-10)12(16)15-11-5-2-6-14-8-11/h1-8H,13H2,(H,15,16)

25844-48-8SDS

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-amino-N-pyridin-3-ylbenzamide

1.2 Other means of identification

Product number -
Other names 3-Amino-N-pyridin-3-yl-benzamide

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:25844-48-8 SDS

25844-48-8Relevant academic research and scientific papers

Anthracene appended pyridinium amide-urea conjugate in selective fluorometric sensing of L-N-acetylvaline salt

Ghosh, Kumaresh,Sarkar, Tanmay,Chattopadhyay, Asoke P.

supporting information; experimental part, p. 1211 - 1218 (2011/03/22)

A new anthracene labeled pyridinium amide-urea conjugate 1 has been designed and synthesized. The receptor shows a different fluorometric response with L-N-acetylvaline and L-N-acetylalanine salts in CH3CN in contrast to the other salts of L-N-

Exploration of secondary and tertiary pharmacophores in unsymmetrical N,N′-diaryl urea inhibitors of soluble epoxide hydrolase

Anandan, Sampath-Kumar,Gless, Richard D.

scheme or table, p. 2740 - 2744 (2010/07/15)

The impact of various secondary and tertiary pharmacophores on in vitro potency of soluble epoxide hydrolase (sEH) inhibitors based on the unsymmetrical urea scaffold 1 is discussed. N,N′-Diaryl urea inhibitors of soluble epoxide hydrolase exhibit subtle variations in inhibitory potency depending on the secondary pharmacophore but tolerate considerable structural variation in the second linker/tertiary pharmacophore fragment.

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