Cas 1375476-66-6,1-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone

1375476-66-6

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Basic information

Product Name: 1-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone
Synonyms: 1-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone
CAS NO:1375476-66-6
Molecular Formula:
Molecular Weight: 392.38
EINECS: N/A
Product Categories: N/A
Mol File: 1375476-66-6.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-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone(1375476-66-6)
EPA Substance Registry System: 1-phenyl-2-(phenylimino)-2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanone(1375476-66-6)

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: 1375476-66-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1375476-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,4,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1375476-66:
(9*1)+(8*3)+(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*6)+(1*6)=196
196 % 10 = 6
So 1375476-66-6 is a valid CAS Registry Number.

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1375476-66-6Relevant articles and documents

Copper-catalyzed C-H oxidation/cross-coupling of α-amino carbonyl compounds

Wu, Ji-Cheng,Song, Ren-Jie,Wang, Zhi-Qiang,Huang, Xiao-Cheng,Xie, Ye-Xiang,Li, Jin-Heng

, p. 3453 - 3457 (2012)

Keeping options open: The new and mild title reaction involving indoles selectively furnishes 1 and 2 with the aid of tert-butyl hydroperoxide (TBHP). The method represents the first example of a copper-catalyzed α arylation of α-amino carbonyl substrates leading to α-aryl α-imino and α-aryl α-oxo carbonyl compounds using a C-H oxidation strategy. Copyright

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