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26074-53-3

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26074-53-3 Usage

General Description

2-BROMO-2-ETHYLBUTYRYL BROMIDE is a chemical compound with the molecular formula C8H15Br2O. It is a colorless to light yellow liquid with a pungent odor. 2-BROMO-2-ETHYLBUTYRYL BROMIDE is primarily used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It is also used in the production of fine chemicals, such as flavors and fragrances. Additionally, 2-BROMO-2-ETHYLBUTYRYL BROMIDE is used as an intermediate in the synthesis of other organic compounds. It should be handled and stored with care, as it is corrosive and can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 26074-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,7 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26074-53:
(7*2)+(6*6)+(5*0)+(4*7)+(3*4)+(2*5)+(1*3)=103
103 % 10 = 3
So 26074-53-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10Br2O/c1-3-6(8,4-2)5(7)9/h3-4H2,1-2H3

26074-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-ethylbutanoyl bromide

1.2 Other means of identification

Product number -
Other names Diaethylbromacetylbromid

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:26074-53-3 SDS

26074-53-3Relevant articles and documents

The synthetic protocol for α-bromocarbonyl compounds via brominations

Murata, Yumi,Takeuchi, Kentaro,Nishikata, Takashi

, p. 2726 - 2736 (2019/04/08)

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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