39563-53-6 Usage
General Description
2-bromodecane is a chemical compound that belongs to the class of organic compounds known as bromoalkanes. It is a colorless liquid with a faint, sweet odor. 2-bromodecane is commonly used as a reagent in organic synthesis and has the potential to be used in various applications in the manufacturing industry. It is known to be a highly flammable and potentially hazardous chemical, requiring careful handling due to its toxic and corrosive properties. Its main use is as an intermediate in the production of other chemicals and pharmaceuticals. In addition, it can be used in the synthesis of polymers and as a solvent in organic reactions. Overall, 2-bromodecane is an important chemical reagent with various industrial and laboratory applications.
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 articles and documents
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.
