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2-bromodecane is a colorless liquid with a faint, sweet odor, belonging to the class of organic compounds known as bromoalkanes. It is a highly flammable and potentially hazardous chemical, requiring careful handling due to its toxic and corrosive properties.

39563-53-6

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39563-53-6 Usage

Uses

Used in Chemical Synthesis:
2-bromodecane is used as a reagent in organic synthesis for the production of other chemicals and pharmaceuticals. It serves as an intermediate in various chemical reactions, contributing to the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
2-bromodecane is used as an intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in Polymer Synthesis:
2-bromodecane is used in the synthesis of polymers, contributing to the development of new materials with specific properties for various applications.
Used as a Solvent in Organic Reactions:
2-bromodecane is used as a solvent in organic reactions, facilitating the process and improving the efficiency of certain chemical transformations.
Used in Manufacturing Industry:
2-bromodecane is used in various applications within the manufacturing industry, including the production of chemicals, pharmaceuticals, and polymers, as well as serving as a solvent in organic reactions. Its versatility as a reagent makes it an important chemical in the industry.

Check Digit Verification of cas no

The CAS Registry Mumber 39563-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,6 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39563-53:
(7*3)+(6*9)+(5*5)+(4*6)+(3*3)+(2*5)+(1*3)=146
146 % 10 = 6
So 39563-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H21Br/c1-3-4-5-6-7-8-9-10(2)11/h10H,3-9H2,1-2H3

39563-53-6Relevant academic research and scientific papers

Regiodivergent Conversion of Alkenes to Branched or Linear Alkylpyridines

Kim, Minseok,Shin, Sanghoon,Koo, Yejin,Jung, Sungwoo,Hong, Sungwoo

supporting information, p. 708 - 713 (2022/01/20)

Herein we report a practical protocol for the visible-light-induced regiodivergent radical hydropyridylation of unactivated alkenes using pyridinium salts. This approach provides a unified synthetic platform to control the regioselectivity of the synthesis of linear or branched C4-alkylated pyridines. A remarkable selectivity switch from the anti-Markovnikov to the Markovnikov product can be achieved by the addition of tetrabutylammonium bromide. The versatility of this protocol is further demonstrated based on the late-stage functionalization in pharmaceuticals.

Carbon tetrabromide - A new brominating agent for alkanes and arylalkanes

Smirnov,Zelikman,Beletskaya,Golubeva,Tsvetkov,Levitskii,Kazankova

, p. 962 - 966 (2007/10/03)

Quantitative catalytic bromination of alkanes, cycloalkanes, and arylalkanes with carbon tetrabromide as brominating agent was accomplished for the first time.

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