Cas 83848-87-7,3-Chloro-benzoic acid 6-hydroxy-2-oxo-1,2,5,6-tetrahydro-4H-imidazo[4,5,1-ij]quinolin-5-yl ester

83848-87-7

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Basic information

Product Name: 3-Chloro-benzoic acid 6-hydroxy-2-oxo-1,2,5,6-tetrahydro-4H-imidazo[4,5,1-ij]quinolin-5-yl ester
Synonyms:
CAS NO:83848-87-7
Molecular Formula:
Molecular Weight: 344.754
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: 3-Chloro-benzoic acid 6-hydroxy-2-oxo-1,2,5,6-tetrahydro-4H-imidazo[4,5,1-ij]quinolin-5-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Chloro-benzoic acid 6-hydroxy-2-oxo-1,2,5,6-tetrahydro-4H-imidazo[4,5,1-ij]quinolin-5-yl ester(83848-87-7)
EPA Substance Registry System: 3-Chloro-benzoic acid 6-hydroxy-2-oxo-1,2,5,6-tetrahydro-4H-imidazo[4,5,1-ij]quinolin-5-yl ester(83848-87-7)

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: 83848-87-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83848-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83848-87:
(7*8)+(6*3)+(5*8)+(4*4)+(3*8)+(2*8)+(1*7)=177
177 % 10 = 7
So 83848-87-7 is a valid CAS Registry Number.

83848-87-7Upstream product

83848-87-7Downstream Products

83848-87-7Relevant academic research and scientific papers

Synthesis and Reactions of Some Dihydro and Tetrahydro-4H-Imidazoquinoline Derivatives

Saari, Walfred S.,Halczenko, Wasyl,Freedman, Mark B.,Arison, Byron H.

, p. 837 - 840 (2007/10/02)

Reaction of phenyl N-(8-quinolyl)carbamate with sodium borohydride afforded 1,2-dihydro-4H-imidazoquinolin-2-one, 2a.The 5,6-double bond of 2a was functionalized by reaction with nitrosyl chloride to give the nitroolefin 4 and by reaction with h

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