Cas 1126897-90-2,2-butyl-5,6-dimethyl-3-{4-(trifluoromethyl)phenyl-1-{4-(trifluoromethyl)benzoyl}}indole

1126897-90-2

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Basic information

Product Name: 2-butyl-5,6-dimethyl-3-{4-(trifluoromethyl)phenyl-1-{4-(trifluoromethyl)benzoyl}}indole
Synonyms:
CAS NO:1126897-90-2
Molecular Formula:
Molecular Weight: 517.514
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: 2-butyl-5,6-dimethyl-3-{4-(trifluoromethyl)phenyl-1-{4-(trifluoromethyl)benzoyl}}indole(CAS DataBase Reference)
NIST Chemistry Reference: 2-butyl-5,6-dimethyl-3-{4-(trifluoromethyl)phenyl-1-{4-(trifluoromethyl)benzoyl}}indole(1126897-90-2)
EPA Substance Registry System: 2-butyl-5,6-dimethyl-3-{4-(trifluoromethyl)phenyl-1-{4-(trifluoromethyl)benzoyl}}indole(1126897-90-2)

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: 1126897-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1126897-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,8,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1126897-90:
(9*1)+(8*1)+(7*2)+(6*6)+(5*8)+(4*9)+(3*7)+(2*9)+(1*0)=182
182 % 10 = 2
So 1126897-90-2 is a valid CAS Registry Number.

1126897-90-2Upstream product

1126897-62-8 5,6-dimethyl-1-{4-(trifluoromethyl)benzoyl}benzotriazole

1126897-90-2Downstream Products

1126897-90-2Relevant academic research and scientific papers

Palladium-catalyzed indolization of N-aroylbenzotriazoles with disubstituted alkynes

Nakamura, Ltaru,Nemoto, Tetsuya,Shiraiwa, Naozumi,Terada, Masahiro

, p. 1055 - 1058 (2009)

The palladium-catalyzed denitrogenative indolization of N-aroylbenzotriazoles 1 and internal alkynes 2 produced the corresponding polysubstituted indoles 3 in good to high yields. For example, the reaction of 5,6-dimethyl-1-[4-(trifluoromethyl)benzoyl]ben

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