Cas 1613036-34-2,(Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline

1613036-34-2

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Basic information

Product Name: (Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline
Synonyms: (Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline
CAS NO:1613036-34-2
Molecular Formula:
Molecular Weight: 502.449
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: (Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline(1613036-34-2)
EPA Substance Registry System: (Z)-2-(4-bromophenyl)-1-(phenyl(trimethylsilyl)methylene)-3-(trifluoromethyl)isoindoline(1613036-34-2)

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: 1613036-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1613036-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,3,0,3 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1613036-34:
(9*1)+(8*6)+(7*1)+(6*3)+(5*0)+(4*3)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 1613036-34-2 is a valid CAS Registry Number.

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1613036-34-2Relevant academic research and scientific papers

One-pot synthesis of trifluoromethylated phthalans via intramolecular cyclization from 2-alkynylbenzaldehydes

Xu, Lijun,Jiang, Haizhen,Hao, Jian,Zhao, Gang

, p. 4373 - 4378 (2014)

An efficient tandem addition/cyclization procedure for the synthesis of trifluoromethylated phthalans under mild conditions was developed. This procedure involves tetrabutylammonium fluoride (TBAF)-promoted addition of Ruppert-Prakash reagent (TMSCF3

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