Cas 145050-06-2,tert-Butyl-[(Z)-3-(2,2-difluoro-5-phenyl-pentyloxy)-propenyl]-diphenyl-silane

145050-06-2

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Basic information

Product Name: tert-Butyl-[(Z)-3-(2,2-difluoro-5-phenyl-pentyloxy)-propenyl]-diphenyl-silane
Synonyms:
CAS NO:145050-06-2
Molecular Formula:
Molecular Weight: 478.698
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: tert-Butyl-[(Z)-3-(2,2-difluoro-5-phenyl-pentyloxy)-propenyl]-diphenyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl-[(Z)-3-(2,2-difluoro-5-phenyl-pentyloxy)-propenyl]-diphenyl-silane(145050-06-2)
EPA Substance Registry System: tert-Butyl-[(Z)-3-(2,2-difluoro-5-phenyl-pentyloxy)-propenyl]-diphenyl-silane(145050-06-2)

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: 145050-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145050-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145050-06:
(8*1)+(7*4)+(6*5)+(5*0)+(4*5)+(3*0)+(2*0)+(1*6)=92
92 % 10 = 2
So 145050-06-2 is a valid CAS Registry Number.

145050-06-2Upstream product

145049-60-1 Imidazole-1-carbothioic acid O-{3-[(Z)-3-(tert-butyl-diphenyl-silanyl)-allyloxy]-2,2-difluoro-1-phenethyl-propyl} ester

145050-06-2Downstream Products

145050-06-2Relevant academic research and scientific papers

Cyclization reactions of β,β-difluoroalkyl radicals (-CF2-C·) for synthesizing gem-difluorocyclic compounds

Morikawa,Kodama,Uchida,Takano,Washio,Taguchi

, p. 8915 - 8926 (2007/10/02)

Cyclization reactions of β,β-difluoroalkyl radicals were carried out. 5 or 6-Exo selective radical cyclizations gave gem-difluorocyclopentane or -cyclohexane derivatives in 53-96% yields. 2,5-Disubstituted-3,3-difluorotetrahydropyran derivatives were prep

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