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56812-60-3

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56812-60-3 Usage

General Description

2-Bromobenzylmagnesium bromide is a chemical compound consisting of a benzene ring that is substituted with a bromine atom and a magnesium atom bonded to the benzyl group. It is a versatile organometallic reagent commonly used in organic synthesis as a Grignard reagent, reacting with various electrophiles such as halides, carbonyl compounds, and epoxides to form new carbon-carbon bonds. This reagent is particularly useful in the formation of carbon-carbon bonds and is widely employed in the synthesis of complex organic molecules and pharmaceuticals. Additionally, it has been utilized in the preparation of various natural products, bioactive compounds, and advanced materials due to its high reactivity and functional group tolerance.

Check Digit Verification of cas no

The CAS Registry Mumber 56812-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56812-60:
(7*5)+(6*6)+(5*8)+(4*1)+(3*2)+(2*6)+(1*0)=133
133 % 10 = 3
So 56812-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Br.BrH.Mg/c1-6-4-2-3-5-7(6)8;;/h2-5H,1H2;1H;/q-1;;+2/p-1

56812-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,1-bromo-2-methanidylbenzene,bromide

1.2 Other means of identification

Product number -
Other names 2-Bromobenzylmagnesium bromide 0.25 M in Diethyl Ether

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:56812-60-3 SDS

56812-60-3Relevant articles and documents

Benzylic Grignard Reagents: Application of (thf = tetrahydrofuran) in Regioselective Grignard Formation and C-O Cleavage in Benzyl Ethers

Gallagher, Michael J.,Harvey, Stephen,Raston, Colin L.,Sue, Rodney E.

, p. 289 - 290 (2007/10/02)

Benzylic Grignard reagents (2)-(4), bearing ortho- and para-halogeno ring substituents, are readily accessible by treating the corresponding benzylic halide with (1) in tetrahydrofuran (thf); o- and p-chloromethyl(methoxymethyl)benzenes with (1) rapidly yield 'di-Grignards' whereas the meta-isomer only affords a mono-Grignard' (5), and bis(methoxymethyl)benzenes slowly undergo C-O cleavage, (6).

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