26074-53-3 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-2-ETHYLBUTYRYL BROMIDE is used as a reagent in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex organic molecules that are integral to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-2-ETHYLBUTYRYL BROMIDE is utilized as a reagent in the preparation of agrochemicals, contributing to the development of compounds that are essential for crop protection and enhancement of agricultural yields.
Used in Fine Chemicals Production:
2-BROMO-2-ETHYLBUTYRYL BROMIDE is employed as a reagent in the production of fine chemicals, specifically in the creation of flavors and fragrances, where its properties allow for the synthesis of a wide range of aromatic compounds.
Used as an Intermediate in Organic Synthesis:
Beyond its direct applications, 2-BROMO-2-ETHYLBUTYRYL BROMIDE serves as an intermediate in the synthesis of other organic compounds, highlighting its versatility and importance in the broader field of organic chemistry.
Safety Considerations:
Given its corrosive nature, 2-BROMO-2-ETHYLBUTYRYL BROMIDE requires careful handling and storage to prevent skin and eye irritation upon contact, emphasizing the need for proper safety measures during its use in various applications.
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
26074-53-3Relevant academic research and scientific papers
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.
