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34696-73-6

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34696-73-6 Usage

Uses

Different sources of media describe the Uses of 34696-73-6 differently. You can refer to the following data:
1. 3,5-Dimethylphenylmagnesium bromide is used as pharmaceutical intermediate.
2. 3,5-Dimethylphenylmagnesium bromide solution can be used:As a starting material for the synthesis of diarylborinic acids, which on Suzuki coupling with vinyl triflate yield penultimate methyl ester.To prepare 3,5-dimethyl-p-terphenyl by reacting with biphenylsulfonate in the presence of dppfNiCl2 catalyst.

Check Digit Verification of cas no

The CAS Registry Mumber 34696-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,9 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34696-73:
(7*3)+(6*4)+(5*6)+(4*9)+(3*6)+(2*7)+(1*3)=146
146 % 10 = 6
So 34696-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H9.BrH.Mg/c1-7-4-3-5-8(2)6-7;;/h4-6H,1-2H3;1H;/q;;+1/p-1/rC8H9BrMg/c1-6-3-7(2)5-8(4-6)10-9/h3-5H,1-2H3

34696-73-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H54057)  3,5-Dimethylphenylmagnesium bromide, 0.5M in 2-MeTHF   

  • 34696-73-6

  • 100ml

  • 1667.0CNY

  • Detail
  • Aldrich

  • (562076)  3,5-Dimethylphenylmagnesiumbromidesolution  0.5 M in THF

  • 34696-73-6

  • 562076-50ML

  • 2,653.56CNY

  • Detail

34696-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,1,3-dimethylbenzene-5-ide,bromide

1.2 Other means of identification

Product number -
Other names 3,5-dimethyphenylmagnesium bromide

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:34696-73-6 SDS

34696-73-6Relevant articles and documents

Room-Temperature Palladium(II)-Catalyzed Direct 2-Arylation of Indoles with Tetraarylstannanes

Liu, Yuxia,Wang, Chao,Huang, Linjuan,Xue, Dong

supporting information, p. 1613 - 1618 (2020/09/15)

A palladium(II)-catalyzed direct 2-arylation of indoles by tetraarylstannanes with oxygen (balloon) as the oxidant at room temperature has been developed. Various tetraarylstannanes can be employed as aryl sources for 2-arylation of indoles in up to 89% yield, providing a practical and efficient catalytic protocol for accessing 2-arylindoles.

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.

CHIRAL PHOSPHORUS COMPOUNDS

-

Page/Page column 28, (2008/12/04)

The present invention provides P-chiral compounds of general formula (II) and (III): wherein at least one of R21, R25, R26 and R30 is independently selected from C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; at least one of R22, R24, R27 and R29 are independently selected from C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy and the remaining substituents selected from R22, R24, R27 and R29 are hydrogen; and R23 and R28 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy; Formula (III): wherein at least one of R21, R25, R26 and R30 is independently selected from phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; and R22, R23, R24, R27, R28 and R29 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy.wherein at least one of R21, R25, R26 and R30 is independently selected from phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; and R22, R23, R24, R27, R28 and R29 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy.

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