75484-32-1 Usage
Uses
Used in Chemical Synthesis:
2-(Chloromethyl)-1,2-epoxybutane is used as an intermediate in the production of other chemicals for various applications. Its high reactivity allows it to react with a variety of substances, making it a crucial component in the synthesis of numerous organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Chloromethyl)-1,2-epoxybutane is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its ability to form new chemical bonds with other molecules makes it an essential component in the development of new drugs and medications.
Used in Agrochemical Industry:
2-(Chloromethyl)-1,2-epoxybutane is also utilized in the agrochemical industry as an intermediate for the synthesis of various agrochemical products. Its reactivity enables the creation of new compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals.
Due to the potential health hazards associated with 2-(Chloromethyl)-1,2-epoxybutane, it is crucial to follow proper handling and storage procedures when working with 2-(Chloromethyl)-1,2-epoxybutane.
Check Digit Verification of cas no
The CAS Registry Mumber 75484-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,8 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75484-32:
(7*7)+(6*5)+(5*4)+(4*8)+(3*4)+(2*3)+(1*2)=151
151 % 10 = 1
So 75484-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClO/c1-2-5(3-6)4-7-5/h2-4H2,1H3
75484-32-1Relevant academic research and scientific papers
Synthesis and characterisation of thioether functionalised gallium and indium alkoxides
Barth, Sven,Biegger, Felix,Puchberger, Michael
supporting information, p. 16439 - 16445 (2015/09/28)
This paper provides evidence of formerly unknown thioether coordination in metal alkoxides. The thioether functionalised alkanols serving as alcoholate ligands have been prepared by a generic route. The gallium and indium alkoxides provide the first evidence for sulphur coordination in the liquid and solid state in metal alkoxide derivatives. The presence of amines suppresses the coordination of thioether moieties leading to a well-known bonding mode in aminoalcoholates.
Reactions of 2-substituted epichlorohydrins
Tanyeli,Demir,Akhmedov,Ozgul,Kandemir
, p. 2967 - 2980 (2007/10/03)
2-Substituted epichlorohydrins have been synthesized by starting with 1,2-dichloro acetone and various alkyl and aryl halides via dichlorohydrins followed by cyclization. The reactive 2-substituted epichlorohydrins were subjected to nucleophilic attacking of azide and cyanide ions to afford corresponding β-azido alcohols and α,β-unsaturated nitriles.
