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1493-86-3

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1493-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1493-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1493-86:
(6*1)+(5*4)+(4*9)+(3*3)+(2*8)+(1*6)=93
93 % 10 = 3
So 1493-86-3 is a valid CAS Registry Number.

1493-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,3,3-tetrafluoro-1-phenylprop-1-enyl)benzene

1.2 Other means of identification

Product number -
Other names 2,3,3,3-Tetrafluor-1,1-diphenyl-propen

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:1493-86-3 SDS

1493-86-3Relevant articles and documents

From C1 to C3: Copper-Catalyzed gem-Bis(trifluoromethyl)olefination of α-Diazo Esters with TMSCF3

Hu, Jinbo,Hu, Mingyou,Liu, Qinghe,Ni, Chuanfa,Pan, Shitao,Wang, Qian,Xie, Qiqiang

, p. 8507 - 8511 (2020)

A Cu-catalyzed gem-bis(trifluoromethyl)olefination of α-diazo esters, using TMSCF3 as the only fluorocarbon source, has been developed and provides an exquisite method to access gem-bis(trifluoromethyl)alkenes. This unprecedented olefination pr

Mild and metal-free trifluoromethylation and pentafluoroethylation of gem-difluoroalkenes with TMSCF3 and TMSCF2CF3

Jin, Guanyi,Zhang, Xuxue,Fu, Dan,Dai, Wenpeng,Cao, Song

, p. 7892 - 7899 (2015/09/15)

A direct and efficient approach for the trifluoromethylation and pentafluoroethylation of 1,1-diaryl-2,2-difluoroethenes with TMSCF3 and TMSCF2CF3 in the presence of TBAF was developed. The reactions proceeded smoothly und

On the reactions of trifluorovinylsilanes with aromatic ketones - Expected and some unexpected results

Kirij,Dontsova,Pavlenko,Yagupolskii,Tyrra,Naumann

experimental part, p. 184 - 189 (2010/04/30)

The reactions of aromatic ketones with trialkyl(trifluorovinyl)silanes in the presence of fluoride ions were studied. The conditions for the selective addition of trialkyl(trifluorovinyl)silanes to the carbonyl function of aromatic ketones in the presence

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