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Magnesium, dibromo-m-1,2-ethynediyldi-, also known as magnesium dibromide ethynediyl, is an inorganic compound with the chemical formula C2Br2Mg. It is a colorless solid that is highly sensitive to moisture and air, making it a potentially hazardous substance. Magnesium, dibromo-m-1,2-ethynediyldi- is formed by the reaction of magnesium metal with 1,4-dibromobutadiyne, resulting in the formation of a magnesium-carbon triple bond. It is used as a reagent in organic synthesis, particularly in the preparation of various organic compounds containing the C≡C triple bond. Due to its reactivity, it is essential to handle Magnesium, dibromo-m-1,2-ethynediyldi- with extreme caution and under controlled conditions to prevent unwanted reactions or hazards.

4301-15-9

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4301-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4301-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4301-15:
(6*4)+(5*3)+(4*0)+(3*1)+(2*1)+(1*5)=49
49 % 10 = 9
So 4301-15-9 is a valid CAS Registry Number.

4301-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name acetylene-bis-magnesium bromide

1.2 Other means of identification

Product number -
Other names acetylene dimagnesium 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:4301-15-9 SDS

4301-15-9Relevant academic research and scientific papers

Mechanism of the reaction of acetylene with Grignard reagents

Paellin, Vello,Otsa, Enn,Tuulmets, Ants

, p. 149 - 152 (2007/10/03)

Kinetics of the reaction between acetylene and phenylmagnesium bromide were investigated in diethyl ether in the presence of small additions of triethylamine and without a catalyst. The mechanistic scheme suggested by Grignard et al. was supplemented with the reaction of bromomagnesiumacetylene with the Grignard reagent. The rate constants for individual reactions were determined. Triethylamine catalyzes the reactions to different extents, the conversions of bromomagnesiumacetylene being the most susceptible to the catalysis. The possible ways of the action of the catalyst were discussed and the importance of nucleophilic assistance was stressed.

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