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Benzenamine, N,N-dimethyl-4-(trifluoroethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134959-15-2

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134959-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134959-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134959-15:
(8*1)+(7*3)+(6*4)+(5*9)+(4*5)+(3*9)+(2*1)+(1*5)=152
152 % 10 = 2
So 134959-15-2 is a valid CAS Registry Number.

134959-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-4-(1,2,2-trifluoroethenyl)aniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N,N-dimethyl-4-(trifluoroethenyl)

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:134959-15-2 SDS

134959-15-2Downstream Products

134959-15-2Relevant academic research and scientific papers

METHOD FOR PRODUCING SUBSTITUTED FLUORINE-CONTAINING OLEFIN

-

Page/Page column 11, (2013/02/28)

This invention relates to a method of reacting fluoroolefin with an organic magnesium compound in the presence of a catalyst comprising nickel or palladium so as to efficiently produce fluoroolefin, such as TFE, in which a fluorine (F) atom or atoms bonded to the sp2 hybridized carbon atom are substituted with an organic group.

Palladium-catalyzed coupling reactions of tetrafluoroethylene with arylzinc compounds

Ohashi, Masato,Kambara, Tadashi,Hatanaka, Tsubasa,Saijo, Hiroki,Doi, Ryohei,Ogoshi, Sensuke

supporting information; experimental part, p. 3256 - 3259 (2011/04/24)

Organofluorine compounds are widely used in all aspects of the chemical industry. Although tetrafluoroethylene (TFE) is an example of an economical bulk organofluorine feedstock, the use of TFE is mostly limited to the production of poly(tetrafluoroethylene) and copolymers with other alkenes. Furthermore, no catalytic transformation of TFE that involves carbon-fluorine bond activation has been reported to date. We herein report the first example of a palladium-catalyzed coupling reaction of TFE with arylzinc reagents in the presence of lithium iodide, giving α,β,β-trifluorostyrene derivatives in excellent yields.

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