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Mercury, bromo(1-methylpropyl)-, also known as bromo(1-methylpropyl)mercury or (1-methylpropyl)mercury bromide, is an organomercury compound with the chemical formula C4H9HgBr. It is a colorless liquid at room temperature and is highly toxic due to its mercury content. Mercury, bromo(1-methylpropyl)- is used as a reagent in organic synthesis and as a catalyst in certain chemical reactions. It is important to handle this substance with extreme care, as exposure to even small amounts can lead to severe health issues, including neurological damage. Due to its hazardous nature, it is subject to strict regulations and is typically used in well-controlled laboratory settings.

868-82-6

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868-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868-82-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 868-82:
(5*8)+(4*6)+(3*8)+(2*8)+(1*2)=106
106 % 10 = 6
So 868-82-6 is a valid CAS Registry Number.

868-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bromo(butan-2-yl)mercury

1.2 Other means of identification

Product number -
Other names sec.-Butyl-mercuri-bromid

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:868-82-6 SDS

868-82-6Downstream Products

868-82-6Relevant academic research and scientific papers

OXIDATIVE TRITYLDEMERCURATION OF ORGANOMERCURY COMPOUNDS

Uglova, E. V.,Makhaev, V. D.,Reutov, O. A.

, p. 1386 - 1389 (2007/10/02)

In the reactions of Ph3CX (X=Cl, Br) with dialkylmercury compounds containing β-hydrogen atoms in the presence of oxygen the main result is determined by competition between two processes, i.e., β elimination (intermolecular hydride transfer) and oxidation with the formation of the peroxide Ph3COOAlk.By variation in the conditions of the reaction between dialkylmercury and triphenylbromomethane a method was found for the production of alkyl triphenylmethyl peroxides containing various primary and secondary alkyl radicals.The stereochemistry was investigated, and the mechanism of the formation of alkyl triphenylmethyl peroxides is discussed.

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