Cas 1032467-73-4,2-amino-1-(3-chloro-4-fluorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydro-4-(4-methylphenyl)-5-oxo-quinoline-3-carbonitrile

1032467-73-4

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Basic information

Product Name: 2-amino-1-(3-chloro-4-fluorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydro-4-(4-methylphenyl)-5-oxo-quinoline-3-carbonitrile
Synonyms:
CAS NO:1032467-73-4
Molecular Formula:
Molecular Weight: 435.929
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-1-(3-chloro-4-fluorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydro-4-(4-methylphenyl)-5-oxo-quinoline-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-1-(3-chloro-4-fluorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydro-4-(4-methylphenyl)-5-oxo-quinoline-3-carbonitrile(1032467-73-4)
EPA Substance Registry System: 2-amino-1-(3-chloro-4-fluorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydro-4-(4-methylphenyl)-5-oxo-quinoline-3-carbonitrile(1032467-73-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1032467-73-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032467-73-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,4,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1032467-73:
(9*1)+(8*0)+(7*3)+(6*2)+(5*4)+(4*6)+(3*7)+(2*7)+(1*3)=124
124 % 10 = 4
So 1032467-73-4 is a valid CAS Registry Number.

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1032467-73-4Relevant academic research and scientific papers

Uncatalyzed and solvent-free process for the synthesis of 1,4-diarylquinoline derivatives

Wang, Xiang-Shan,Zhang, Mei-Mei,Jiang, Hong,Yao, Chang-Sheng,Tu, Shu-Jiang

, p. 1355 - 1364 (2008)

The uncatalyzed and three-component reaction of arylaldehyde, malonodinitrile, and 3-arylamino-5,5-dimethylcyclohex-2-enone at 160°C under solvent-free conditions gave 1,4-diarylquinoline derivatives in high yields. Copyright Taylor & Francis Group, LLC.

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