Cas 939288-33-2,1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione

939288-33-2

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Basic information

Product Name: 1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione
Synonyms: 1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione
CAS NO:939288-33-2
Molecular Formula:
Molecular Weight: 379.886
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: 1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(939288-33-2)
EPA Substance Registry System: 1-(2-chlorophenyl)-7,7-dimethyl-4-phenyl-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione(939288-33-2)

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: 939288-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 939288-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,2,8 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 939288-33:
(8*9)+(7*3)+(6*9)+(5*2)+(4*8)+(3*8)+(2*3)+(1*3)=222
222 % 10 = 2
So 939288-33-2 is a valid CAS Registry Number.

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939288-33-2Downstream Products

939288-33-2Relevant academic research and scientific papers

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

supporting information, p. 1133 - 1137 (2013/02/23)

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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