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Benzene, 1,1'-(1,2,2-trifluoroethylidene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14090-30-3

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14090-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14090-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,9 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14090-30:
(7*1)+(6*4)+(5*0)+(4*9)+(3*0)+(2*3)+(1*0)=73
73 % 10 = 3
So 14090-30-3 is a valid CAS Registry Number.

14090-30-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-diphenyl-1,2,2-trifluoroethane

1.2 Other means of identification

Product number -
Other names 1,2,2-trifluoro-1,1-diphenylethane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14090-30-3 SDS

14090-30-3Downstream Products

14090-30-3Relevant academic research and scientific papers

Utility of silicon tetrafluoride as a catalyst of reactions with xenon difluoride: Fluorinations of phenyl alkenes and benzaldehydes

Tamura, Masanori,Takagi, Toshiyuki,Quan, Heng-Dao,Sekiya, Akira

, p. 163 - 166 (2007/10/03)

Application of silicon tetrafluoride to fluorinations with xenon difluoride as a catalyst is investigated. It was found that vic-difluorination of phenyl alkenes and transformation of benzaldehydes to difluoromethoxybenzenes using xenon difluoride are enhanced by silicon tetrafluoride.

N-Fluorobisimides: Reactions with Some Olefins via α-Fluoro Carbocationic Intermediates

DesMarteau, Darryl D.,Xu, Ze-Qi,Witz, Michael

, p. 629 - 635 (2007/10/02)

N-Fluorobisimides are a new class of electrophilic fluorinating agents.Reaction of (CF3SO2)2NF (1) with olefins gave various products, depending on the reaction conditions and the structure of the substrate.In solvents of higher nucleophilicity such as H2O, acetic acid, aqueous HCl, and (HF)nPy, α-fluorohydrins and their acetates, α,β-chlorofluoro- and α,β-difluoroalkanes were obtained.In acetic acid, trans-stilbene and tetraphenylethylene produced the rearranged, nonfluorinated aldehyde and ketone.Evidence is presented for the reactions proceeding via a one-electron transfer mechanism involving α-fluorocarbocationic intermediates.

FLUORINATION WITH CAESIUM FLUOROXYSULPHATE. ROOM TEMPERATURE FLUORINATION OF PHENYL SUBSTITUTED OLEFINS

Stavber, Stojan,Zupan, Marko

, p. 5035 - 5044 (2007/10/02)

Room -temperature fluorination of 1,1-diphenylethene with caesium fluoroxysulphate in methylene chloride resulted in an addition elimination process, thus yielding 1,1-diphenyl-2-fluoroethene, while in the presence of nucleophile containing species, i.e.,

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