Cas 1402597-41-4,8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one

1402597-41-4

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Basic information

Product Name: 8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one
Synonyms: 8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one
CAS NO:1402597-41-4
Molecular Formula:
Molecular Weight: 467.354
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: 8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one(CAS DataBase Reference)
NIST Chemistry Reference: 8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one(1402597-41-4)
EPA Substance Registry System: 8-chloro-15a-(4-chlorophenyl)-5H-diindolo[1,2-a:3',2'-c]quinolin-15(15aH)-one(1402597-41-4)

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: 1402597-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1402597-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,5,9 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1402597-41:
(9*1)+(8*4)+(7*0)+(6*2)+(5*5)+(4*9)+(3*7)+(2*4)+(1*1)=144
144 % 10 = 4
So 1402597-41-4 is a valid CAS Registry Number.

1402597-41-4Upstream product

1211-35-4 2-(4-chlorophenyl)-1H-indole

1402597-41-4Downstream Products

1402597-41-4Relevant academic research and scientific papers

Copper-catalyzed activation of dioxygen: Oxidative cyclization of 2-arylindoles

Sang, Peng,Xie, Yongju,Zou, Jianwei,Zhang, Yuhong

supporting information; experimental part, p. 1873 - 1878 (2012/10/07)

A series of unusual six-ring-fused heterocycles containing indole and quinoline skeletons was successfully synthesized by a copper-catalyzed reaction from 2-arylated indoles. Two new bonds were regioselectively formed from C-H and C-H coupling. 18O-Labelled experiments revealed that the dioxygen is not only the oxidant but also the reactant. Copyright

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