Cas 1418135-65-5,1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene

1418135-65-5

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Basic information

Product Name: 1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene
Synonyms: 1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene
CAS NO:1418135-65-5
Molecular Formula:
Molecular Weight: 409.408
EINECS: N/A
Product Categories: N/A
Mol File: 1418135-65-5.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: 1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene(CAS DataBase Reference)
NIST Chemistry Reference: 1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene(1418135-65-5)
EPA Substance Registry System: 1,1-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-2-phenyl-1H-indene(1418135-65-5)

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: 1418135-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1418135-65-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,8,1,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1418135-65:
(9*1)+(8*4)+(7*1)+(6*8)+(5*1)+(4*3)+(3*5)+(2*6)+(1*5)=145
145 % 10 = 5
So 1418135-65-5 is a valid CAS Registry Number.

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1418135-65-5Relevant articles and documents

Reusable visible light photoredox catalysts; Catalyzed benzylic C(sp 3)-H functionalization/carbocyclization reactions

Xia, Jia-Dong,Deng, Guo-Bo,Zhou, Ming-Bo,Liu, Wei,Xie, Peng,Li, Jin-Heng

supporting information, p. 2707 - 2713,7 (2012/12/12)

The C(sp3)-H functionalization/carbocyclization reaction through the oxidative quenching of visible light photoredox catalysts is established for constructing functionalized 1H-indenes. The process is general for a wide range of benzylic C(sps

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