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(3 5 BIS(TRIFLUOROMETHYL)PHENYL)MAGNESI& is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112981-69-8

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112981-69-8 Usage

Chemical Properties

Dark brown solution

Check Digit Verification of cas no

The CAS Registry Mumber 112981-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,8 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112981-69:
(8*1)+(7*1)+(6*2)+(5*9)+(4*8)+(3*1)+(2*6)+(1*9)=128
128 % 10 = 8
So 112981-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H3F6.BrH.Mg/c9-7(10,11)5-2-1-3-6(4-5)8(12,13)14;;/h2-4H;1H;/q-1;;+2/p-1

112981-69-8 Well-known Company Product Price

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  • Aldrich

  • (639052)  3,5-Bis(trifluoromethyl)phenylmagnesiumbromidesolution  0.5 M in THF

  • 112981-69-8

  • 639052-50ML

  • 1,086.93CNY

  • Detail

112981-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,1,3-bis(trifluoromethyl)benzene-5-ide,bromide

1.2 Other means of identification

Product number -
Other names 3,5-di-CF3-PhMgBr

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:112981-69-8 SDS

112981-69-8Relevant academic research and scientific papers

Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene- based chiral sulfides as organocatalysts

Huang, Meng-Ting,Wu, Hsin-Yi,Chein, Rong-Jie

supporting information, p. 1101 - 1103 (2014/01/17)

This work describes catalytic and asymmetric aziridinations (15 examples, 95-98% ee) of benzyl bromide and imines via the imino Corey-Chaykovsky reaction using (thiolan-2-yl)diarylmethanol benzyl ether as an organocatalyst. The catalyst and analogues thereof were prepared through an expeditious and efficient synthetic route featuring a double nucleophilic substitution and Shi epoxidation as key steps.

PROCESS FOR THE PREPARATION 3,5-BIS(TRIFLUOROMETHYL)BENZYLALCOHOL

-

Page/Page column 6-7, (2010/02/11)

The present invention concerns a process for preparing 3,5bis(trifluoromethyl)benzylalcohol by formylation in a solvent of an appropriate organo-magnesium derivative with solid paraformaldehyde and optionally its conversion into a 3,5-bis(trifluoromethyl)benzyl halide.

Quinoline derivatives and organic electroluminescent devices

-

, (2008/06/13)

Quinoline derivatives represented by formula (1) wherein two or more of substituents R1 to R7 are each a group of formula (2). It is preferable that among the substituents R1 to R7, at least one of the substituents other than those of general formula (2) be an electron-whithdrawing group. In general formula (2), Q is a carbo- or hetero-aryl group; at least one of the substituents RQ on the group Q is preferably an electron-donating group; and the number (n) of double bonds is preferably 1 to 3. Use of such derivatives in an organic EL device provided with a layer of an organic compound and two electrodes sandwiching the layer as the organic compound gives devices emitting yellow to red light with high brightness and high efficiency. Further, doping a hole transport layer with such derivatives realizes organic EL devices capable of emitting lights of resultant colors (e. g., white) composed of lights from light-emitting and hole transport layers.

Process for the synthesis of 1-(3,5-bis(trifluoromethyl)-phenyl)ethan-1-one

-

Example 2, (2008/06/13)

The present invention is concerned with a novel process for the preparation of 1-(3,5-bis(trifluromethyl)phenyl)ethan-1-one (CAS 30071-93-3). This compound is useful as an intermediate in the synthesis of therapeutic agents.

Triarylphosphine oxide derivatives containing fluorine substituents

-

Example 1, (2010/01/30)

The invention relates to triarylphosphine oxide derivatives containing fluorine substituents that are useful as a monomer in preparation of polymers with improved properties such as chemical resistance and electrical insulating property as well as adhesiveness and flame retardancy. The triarylphosphine oxide derivatives containing fluorine substituents are represented by the chemical formula1: wherein R1and R2are independently a fluorine-substituted alkyl group; and X is hydrogen, a nitro group, or an amine group.

Selective asymmetric hydrogenation of dehydroamino acid derivatives using rhodium and iridium diphosphinite carbohydrate catalyst compositions

-

, (2008/06/13)

A process and catalyst composition are provided for the highly efficient enantioselective hydrogenation of dehydroamino acid derivatives. The catalyst composition comprises rhodium or iridium and a diphosphinite carbohydrate ligand, wherein the phosphorous atoms are attached to aromatic groups substituted with electron-donating substituents. Also provided is a means to selectively produce α amino acids in either the L or the D form, based upon use of a sugar in the ligand with phosphinites attached in an absolute Right-Left or Left-Right configuration, respectively.

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