Cas 1204248-12-3,2-amino-4-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile

1204248-12-3

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Basic information

Product Name: 2-amino-4-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile
Synonyms: 2-amino-4-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile
CAS NO:1204248-12-3
Molecular Formula:
Molecular Weight: 359.428
EINECS: N/A
Product Categories: N/A
Mol File: 1204248-12-3.mol
Article Data: 1

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-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(1204248-12-3)
EPA Substance Registry System: 2-amino-4-(2-furyl)-7,7-dimethyl-5-oxo-1-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile(1204248-12-3)

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: 1204248-12-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1204248-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,2,4 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1204248-12:
(9*1)+(8*2)+(7*0)+(6*4)+(5*2)+(4*4)+(3*8)+(2*1)+(1*2)=103
103 % 10 = 3
So 1204248-12-3 is a valid CAS Registry Number.

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1204248-12-3Relevant articles and documents

Synthesis of N -Aryl-4-arylhexahydroquinoline Derivatives by Reaction of Cyclic Enaminones with Arylidenemalononitriles in DMSO

Han, Wei,Inoue, Chika,Onizawa, Tsunaki,Oriyama, Takeshi

, p. 1495 - 1502 (2020/12/23)

The reaction of cyclic enaminones with arylidenemalono nitriles was carried out in the presence of 13X molecular sieves in dimethyl sulfoxide. Under these mild reaction conditions, various bioactive N -aryl-4-arylhexahydroquinoline derivatives were obtain

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