928-50-7 Usage
Uses
Used in Pharmaceutical Industry:
5-CHLORO-1-PENTENE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 5-CHLORO-1-PENTENE is utilized as a reactant in the production of agrochemicals, playing a role in the development of compounds that can protect crops and enhance agricultural productivity.
Used in Specialty Chemicals Production:
5-CHLORO-1-PENTENE is employed as a building block in the synthesis of specialty chemicals, where its unique properties allow for the creation of tailored chemical products for specific industrial applications.
Used in Polymer Production:
5-CHLORO-1-PENTENE is used as a monomer or reactant in the production of polymers, contributing to the development of materials with specific properties required for various applications.
Used in Organic Synthesis Reactions:
5-CHLORO-1-PENTENE is utilized in organic synthesis reactions, where it can undergo various chemical transformations to produce a wide array of organic compounds for different uses.
Check Digit Verification of cas no
The CAS Registry Mumber 928-50-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 928-50:
(5*9)+(4*2)+(3*8)+(2*5)+(1*0)=87
87 % 10 = 7
So 928-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H9Cl/c1-2-3-4-5-6/h2H,1,3-5H2
928-50-7Relevant academic research and scientific papers
Thermal and induced decompositions of N′-alkoxycarbonyldihydropyridines: End product analysis and EPR spectra of azacyclohexadienyl radicals
Baguley, Paul A.,Walton, John C.
, p. 1423 - 1429 (2007/10/03)
Hydrogen abstraction from N-alkoxycarbonyldihydropyridines generated azacyclohexadienyl radicals (pyridinyl radicals) which are characterised by EPR spectroscopy. In the presence of peroxide initiators, N-alkoxycarbonyl-1,2-dihydropyridines decomposed with production of pyridine, the corresponding alkyl formate, alkyl benzoate and alkanol being formed as the major products. Absence of cyclised products in experiments with substrates containing hex-5-enyl, pent-4-enyloxy etc. units demonstrates that radical production must be minor and that N-alkoxycarbonylazacyclohexadienyl radicals do not readily undergo ss-scission of the exocyclic N-C bond. The most probable mechanism is a direct 1,2-elimination of formate. The alcohols which accompanied the other products are probably formed by hydrolysis of the formates and benzoates. Analogous chemistry is displayed by N-alkoxycarbonyl-1,4-dihydropyridines at higher temperatures where 1,4-elimination of formate is too rapid for homolytic radical production to compete.
