Cas 4937-83-1,(2-amino-5-chloro-3-nitrophenyl)phenyl-methanone

4937-83-1

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Basic information

Product Name: (2-amino-5-chloro-3-nitrophenyl)phenyl-methanone
Synonyms: (2-amino-5-chloro-3-nitrophenyl)phenyl-methanone
CAS NO:4937-83-1
Molecular Formula:
Molecular Weight: 276.679
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2-amino-5-chloro-3-nitrophenyl)phenyl-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (2-amino-5-chloro-3-nitrophenyl)phenyl-methanone(4937-83-1)
EPA Substance Registry System: (2-amino-5-chloro-3-nitrophenyl)phenyl-methanone(4937-83-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 4937-83-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4937-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4937-83:
(6*4)+(5*9)+(4*3)+(3*7)+(2*8)+(1*3)=121
121 % 10 = 1
So 4937-83-1 is a valid CAS Registry Number.

4937-83-1Upstream product

4937-83-1Downstream Products

573692-40-7 (2,3-diamino-5-chloro-phenyl)-phenyl-methanone

4937-83-1Relevant academic research and scientific papers

Synthesis and SAR of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones related to licostinel (Acea 1021) as NMDA/glycine site antagonists

Zhou, Zhang-Lin,Kher, Sunil M.,Cai, Sui Xiong,Whittemore, Edward R.,Espitia, Stephen A.,Hawkinson, Jon E.,Tran, Minhtam,Woodward, Richard M.,Weber, Eckard,Keana, John F. W.

, p. 1769 - 1780 (2007/10/03)

A series of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones (QXs) related to licostinel (Acea 1021) was synthesized and evaluated as antagonists for the glycine site of the N-methyl-D-asparate (NMDA) receptor. The in vitro potency of these

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