5414-21-1 Usage
Description
5-Bromovaleronitrile is an organic compound with the chemical formula C5H8BrN. It is a clear, colorless to light yellow liquid that serves as a versatile building block in the synthesis of various organic molecules.
Uses
Used in Chemical Synthesis:
5-Bromovaleronitrile is used as a reactant for the production of 5-Bromo-pentanoic acid, which is an important intermediate in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
5-Bromovaleronitrile is used as a key intermediate in the synthesis of benzyl(methyl)amino)pentanenitrile, which is utilized in the production of N-methylcadaverine, a compound with potential applications in the pharmaceutical industry.
Used in Chemical Research:
5-Bromovaleronitrile is employed in the preparation of 1-cyanobutyl-3-alkylbenzimidazolium bromide salt by reacting with various N-alkylbenzimidazoles. This salt has potential applications in chemical research and development.
Used in Organic Synthesis:
5-Bromovaleronitrile is used in the synthesis of tridecanenitrile through a Ni-catalyzed cross-coupling reaction with dioctylzinc in the presence of tetraene and MgBr2. Tridecanenitrile can be further utilized in the production of various organic compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5414-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5414-21:
(6*5)+(5*4)+(4*1)+(3*4)+(2*2)+(1*1)=71
71 % 10 = 1
So 5414-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H8BrN/c6-4-2-1-3-5-7/h1-4H2
5414-21-1Relevant articles and documents
Synthetic Studies on d-Biotin, Part 6:1 An Expeditious and Enantiocontrolled Approach to the Total Synthesis of d-Biotin via a Polymer-Supported Chiral Oxazaborolidine-Catalyzed Reduction of meso-Cyclic Imide Strategy
Chen, Fen-Er,Yuan, Jian-Li,Dai, Hui-Fang,Kuang, Yun-Yan,Chu, Yong
, p. 2155 - 2160 (2007/10/03)
An efficient and highly enantioselective synthesis of d-biotin from the known cis-1,3-dibenzyl-2-imidazolidone-4,5-dicarboxylic acid (5) was accomplished in 48% overall yield. The key reactions in the sequence involve the catalytic enantioselective reduction of meso-cyclic imide 6 using polymer-supported chiral oxazoborolidine, derived from (S)-α,α -diphenylprolinol and polymer-bound sulfonyl chloride, and the installation of the C5 side chain at C4 in the thiolactone 9 via a Ni/C-catalyzed Fukuyama coupling reaction.
Synthesis of pyridine-containing macrocycles by cobalt-mediated trimerization of triply-bonded species
Moretto,Zhang,Maryanoff
, p. 3157 - 3158 (2007/10/03)
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ALKYLATION OF ANIONS ON SOLID INORGANIC SUPPORTS: SYNTHESIS OF NITRILES, ESTERS, PHENOLIC ETHERS AND MONO-C-SUBSTITUTED ACETOACETIC ESTERS.
Bram, G.,Fillebeen-Khan, T.,Geraghty, N.
, p. 279 - 290 (2007/10/02)
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