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106265-07-0

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106265-07-0 Usage

General Description

2-Bromo-2-methylbutanoyl bromide is a chemical compound with the molecular formula C5H8Br2O. It is a colorless liquid with a pungent odor, and it is widely used as a reagent in organic synthesis. This chemical is a useful building block for the preparation of various organic compounds and pharmaceuticals. It is primarily used as an alkylating agent in chemical reactions, and its high reactivity makes it a valuable tool for the modification of organic molecules. 2-Bromo-2-methylbutanoyl bromide is also known for its ability to undergo nucleophilic substitution reactions, making it an important tool for the introduction of the bromine functional group into organic molecules. Overall, this chemical is an important intermediate in the synthesis of various organic compounds and plays a crucial role in organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 106265-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,6 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106265-07:
(8*1)+(7*0)+(6*6)+(5*2)+(4*6)+(3*5)+(2*0)+(1*7)=100
100 % 10 = 0
So 106265-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H8Br2O/c1-3-5(2,7)4(6)8/h3H2,1-2H3

106265-07-0SDS

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 2-Bromo-2-methylbutanoyl bromide

1.2 Other means of identification

Product number -
Other names Butanoyl bromide,2-bromo-2-methyl

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:106265-07-0 SDS

106265-07-0Relevant articles and documents

The synthetic protocol for α-bromocarbonyl compounds via brominations

Murata, Yumi,Takeuchi, Kentaro,Nishikata, Takashi

, p. 2726 - 2736 (2019)

α-Bromocarbonyl compound easily generates α-radicals in the presence of a proper initiator, such as copper salt. Recently, tertiary-alkylation reaction using α-bromocarbonyl compound as a tertiary alkyl source is recognized as one of the most important alkylation reactions. The reactions using α-bromocarbonyl compound are increasing, whereas synthetic methods for various functionalized α-bromocarbonyl compounds are not summarized. Generally, α-bromocarbonyl compounds can be synthesized from the corresponding carboxylic acids via α-bromo acid bromide, but the brominations of carboxylic acids are sometimes problematic. In this paper, we will report some technical information for a bromination and synthetic examples of representative α-bromocarbonyl compounds.

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