Cas 548446-48-6,[2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester

548446-48-6

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Basic information

Product Name: [2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester
Synonyms: [2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester
CAS NO:548446-48-6
Molecular Formula:
Molecular Weight: 489.958
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-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester(548446-48-6)
EPA Substance Registry System: [2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester(548446-48-6)

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: 548446-48-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 548446-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,4,4 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 548446-48:
(8*5)+(7*4)+(6*8)+(5*4)+(4*4)+(3*6)+(2*4)+(1*8)=186
186 % 10 = 6
So 548446-48-6 is a valid CAS Registry Number.

548446-48-6Upstream product

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548446-48-6Relevant academic research and scientific papers

Chemical transformations of 3-amino-2-quinolones

Asis, Silvia E.,Bruno, Ana M.,Dominici, Diego A.,Bollini, Mariela,Gaozza, Carlos H.

, p. 107 - 112 (2007/10/03)

In order to find new antimalarial drugs, an exploration about the chemical properties of the starting compounds 3-amino-6-chloro-4-phenyl-1H-quinolin-2-one (1) and 3-amino-4-methyl-1H-quinolin-2-one (2) was developed. Acylation with acyl chloride, sulfony

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