Cas 339340-72-6,2-amino-4-(4-bromophenyl)-1-(4-fluorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile

339340-72-6

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Basic information

Product Name: 2-amino-4-(4-bromophenyl)-1-(4-fluorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile
Synonyms:
CAS NO:339340-72-6
Molecular Formula:
Molecular Weight: 466.353
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-4-(4-bromophenyl)-1-(4-fluorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-(4-bromophenyl)-1-(4-fluorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(339340-72-6)
EPA Substance Registry System: 2-amino-4-(4-bromophenyl)-1-(4-fluorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(339340-72-6)

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: 339340-72-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 339340-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,3,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 339340-72:
(8*3)+(7*3)+(6*9)+(5*3)+(4*4)+(3*0)+(2*7)+(1*2)=146
146 % 10 = 6
So 339340-72-6 is a valid CAS Registry Number.

339340-72-6Upstream product

339340-72-6Downstream Products

339340-72-6Relevant academic research and scientific papers

A three-component synthesis of N-substituted quinoline-3-carbonitrile derivatives catalysed by L-proline

Shi, Chunling,Chen, Hui,Li, Yan,Shi, Daqing,Ji, Min

experimental part, p. 534 - 537 (2009/04/07)

A series of new N-substituted quinoline-3-carbonitrile derivatives were synthesised by the three-component reaction of N-substituted 5,5-dimethyl-3-aminocyclohex-2-enone, an arylaldehyde, and malononitrile catalysed by L-proline in ethanol at 80°C.

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