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82297-90-3

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82297-90-3 Usage

Uses

3,5-Dichlorophenylmagnesium bromide can be used:In one of the key synthetic steps for the preparation of non-alternant polycyclic hydrocarbon named indeno-benzophenalene.As a substrate in the synthesis of carboxylic esters by reacting with 2-methyl-4,6-pyrimidyl dicarbonates.As a substrate in the synthesis of aryl ketones by reacting with acid chlorides using bis[2-(N,N-dimethylamino)ethyl] ether ligand.

Check Digit Verification of cas no

The CAS Registry Mumber 82297-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82297-90:
(7*8)+(6*2)+(5*2)+(4*9)+(3*7)+(2*9)+(1*0)=153
153 % 10 = 3
So 82297-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2.BrH.Mg/c7-5-2-1-3-6(8)4-5;;/h2-4H;1H;/q;;+1/p-1/rC6H3BrCl2Mg/c7-10-6-2-4(8)1-5(9)3-6/h1-3H

82297-90-3 Well-known Company Product Price

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  • Aldrich

  • (562289)  3,5-Dichlorophenylmagnesiumbromidesolution  0.5 M in THF

  • 82297-90-3

  • 562289-50ML

  • 3,051.36CNY

  • Detail

82297-90-3SDS

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 magnesium,1,3-dichlorobenzene-5-ide,bromide

1.2 Other means of identification

Product number -
Other names 3,5-Dichlorophenylmagnesium bromide solution

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:82297-90-3 SDS

82297-90-3Relevant articles and documents

Synthesis of trifluoromethylated α-hydroxy acids and their derivatives based on alkyl trifluoropyruvates

Vasilyeva,Vorobyeva

, p. 1426 - 1432 (2018/10/31)

The reactions of trifluoropyruvates with nitromethane and arylmagnesium bromides leading to trifluoromethyl-containing α-hydroxy acid esters were studied and various derivatives of the acids were obtained.

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