5398-24-3 Usage
Uses
Used in Organic Synthesis:
2-BROMOBUTYRAMIDE is used as a building block in organic synthesis for its ability to facilitate the creation of a variety of complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of new compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-BROMOBUTYRAMIDE is used as a key intermediate in the synthesis of various drugs. Its presence in the molecular structure can impart specific therapeutic properties, contributing to the development of novel medications.
Used in Agrochemical Industry:
2-BROMOBUTYRAMIDE is also utilized in the agrochemical sector, where it serves as a precursor in the production of different agrochemicals. Its role in this industry is vital for the development of effective crop protection agents and other agricultural products.
Used in Research and Development:
In research and development, 2-BROMOBUTYRAMIDE is employed as a reagent in various chemical experiments and studies. Its unique properties make it an essential tool for understanding and advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 5398-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5398-24:
(6*5)+(5*3)+(4*9)+(3*8)+(2*2)+(1*4)=113
113 % 10 = 3
So 5398-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H8BrNO/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H2,6,7)
5398-24-3Relevant academic research and scientific papers
Switchable Smiles Rearrangement for Enantioselective O-Aryl Amination
Chang, Xihao,Zhang, Qinglin,Guo, Chang
supporting information, p. 4915 - 4918 (2019/06/27)
Asymmetric assembly of atropisomeric anilines from abundant and readily available precursors is one of the most challenging but valuable processes in organic synthesis. The use of highly efficient Smiles rearrangement to accomplish switchable enantioselec
Oxidative Decyanation of Secondary Nitriles to Ketones
Freerksen, Robert W.,Selikson, Sandra J.,Wroble, Randall R.,Kyler, S. Keith,Watt, David S.
, p. 4087 - 4096 (2007/10/02)
Procedures for the oxidative decyanation of secondary nitriles to ketones involve (1) iodination of N-(trialkylsilyl)ketenimines derived from secondary nitriles and subsequent hydrolysis of the α-iodo nitriles with silver oxide, (2) addition of nitrosobenzene to N-(trialkylsilyl)ketenimines, (3) conversion of secondary nitriles to α-(phenylthio) nitriles and subsequent hydrolysis with N-bromosuccinimide in aqueous acetonitrile, and (4) preparation of α-hydroperoxy nitriles by direct oxygenation of anions of secondary nitriles and subsequent reductive hydrolysis with stannous chloride followed by sodium hydroxide.The latter general procedure was applied to various secondary nitriles bearing dialkyl, aryl and alkyl, and diaryl substituents to provide ketones in good yield and was extended to the oxidative decyanation of α,β-unsaturated nitriles to furnish α,β-unsaturated ketones.
