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132856-34-9

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132856-34-9 Usage

Common Use

Reagent in organic synthesis

Application

Grignard reactions

Reaction Type

Addition reaction to carbonyl group

Function

Forms new carbon-carbon bonds

Versatility

Can synthesize various organic compounds

Reactivity

High reactivity

Selectivity

Known for its selectivity

Importance

Essential for complex organic molecule synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 132856-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132856-34:
(8*1)+(7*3)+(6*2)+(5*8)+(4*5)+(3*6)+(2*3)+(1*4)=129
129 % 10 = 9
So 132856-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13.ClH.Mg/c1-7-5-8(2)10(4)9(3)6-7;;/h5-6H,4H2,1-3H3;1H;/q;;+1/p-1/rC10H13ClMg/c1-7-4-8(2)10(6-12-11)9(3)5-7/h4-5H,6H2,1-3H3

132856-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,2-methanidyl-1,3,5-trimethylbenzene,chloride

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethylbenzylmagnesium chloride 0.25 M in Tetrahydrofuran

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:132856-34-9 SDS

132856-34-9Downstream Products

132856-34-9Relevant articles and documents

Nickel-Catalyzed Cross-Coupling of Anisoles with Alkyl Grignard Reagents via C-O Bond Cleavage

Tobisu, Mamoru,Takahira, Tsuyoshi,Chatani, Naoto

, p. 4352 - 4355 (2015)

Nickel-catalyzed cross-coupling of methoxyarenes with alkyl Grignard reagents, which involves the cleavage of the C(aryl)-OMe bond, has been developed. The use of 1,3-dicyclohexylimidazol-2-ylidene as a ligand allows the introduction of a variety of alkyl groups, including Me, Me3SiCH2, ArCH2, adamantyl, and cyclopropyl. The method can also be used for the alkylative elaboration of complex molecules bearing a C(aryl)-OMe bond.

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