Cas 1354541-87-9,(2-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane

1354541-87-9

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Basic information

Product Name: (2-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane
Synonyms: (2-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane
CAS NO:1354541-87-9
Molecular Formula:
Molecular Weight: 582.743
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-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane(CAS DataBase Reference)
NIST Chemistry Reference: (2-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane(1354541-87-9)
EPA Substance Registry System: (2-fluoro-2,2-bis(phenylsulfonyl)-1-(2,4,6-trimethoxyphenyl)ethoxy)trimethylsilane(1354541-87-9)

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: 1354541-87-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1354541-87-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,4,5,4 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1354541-87:
(9*1)+(8*3)+(7*5)+(6*4)+(5*5)+(4*4)+(3*1)+(2*8)+(1*7)=159
159 % 10 = 9
So 1354541-87-9 is a valid CAS Registry Number.

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1354541-87-9Relevant academic research and scientific papers

Facile synthesis of α-monofluoromethyl alcohols: Nucleophilic monofluoromethylation of aldehydes using TMSCF(SO2Ph)2

Prakash, G.K. Surya,Shao, Nan,Zhang, Zhe,Ni, Chuanfa,Wang, Fang,Haiges, Ralf,Olah, George A.

experimental part, p. 27 - 32 (2012/02/05)

α-Fluoromethyl phenyl sulfone derivatives have been extensively employed in various reactions as versatile fluoromethylating reagents. While nucleophilic monofluoromethylations of aldehydes have been achieved using fluoromethyl phenyl sulfone or fluorobis

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