Cas 1417794-70-7,1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione

1417794-70-7

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Basic information

Product Name: 1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione
Synonyms: 1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione
CAS NO:1417794-70-7
Molecular Formula:
Molecular Weight: 347.414
EINECS: N/A
Product Categories: N/A
Mol File: 1417794-70-7.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: 1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(1417794-70-7)
EPA Substance Registry System: 1-(4-methoxyphenyl)-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(1417794-70-7)

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: 1417794-70-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1417794-70-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,7,9 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1417794-70:
(9*1)+(8*4)+(7*1)+(6*7)+(5*7)+(4*9)+(3*4)+(2*7)+(1*0)=187
187 % 10 = 7
So 1417794-70-7 is a valid CAS Registry Number.

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1417794-70-7Relevant articles and documents

NHC-catalyzed cascade synthesis of 1-substituted 4-aryl- tetrahydroquinoline-2,5-diones

Yao, Changsheng,Jiao, Weihui,Xiao, Zhaoxin,Liu, Rui,Li, Tuanjie,Yu, Chenxia

, p. 1133 - 1137 (2013)

N-Heterocyclic carbene (NHC)-catalyzed organocascade reactions via redox processes were found to be a simple and flexible procedure for the synthesis of a series of suitably functionalized 1-substituted 4-aryl-tetrahydroquinoline-2, 5-diones. A wide range of potential biologically active quinoline derivatives for biomedical screening were obtained.

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