4401-11-0 Usage
Uses
Used in Pharmaceutical Industry:
2-Acetyloxirane is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications. Its reactivity and versatility allow for the creation of a wide range of molecular structures, enhancing the therapeutic potential of resulting compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Acetyloxirane is utilized as a precursor in the production of various agrochemicals, including pesticides and herbicides. Its role in these applications aids in the development of more effective and targeted agricultural chemicals, supporting crop protection and yield enhancement.
Used as a Solvent in Organic Synthesis:
2-Acetyloxirane is employed as a solvent in organic synthesis processes, facilitating reactions and improving the efficiency of chemical transformations. Its properties as a solvent make it suitable for a range of applications, broadening its utility in the chemical industry.
Used as a Reagent in Organic Synthesis:
As a reagent, 2-Acetyloxirane is instrumental in various organic synthesis reactions, enabling the formation of new chemical bonds and the construction of complex molecular structures. Its reactivity and functional group compatibility make it a valuable component in the synthesis of diverse organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 4401-11-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4401-11:
(6*4)+(5*4)+(4*0)+(3*1)+(2*1)+(1*1)=50
50 % 10 = 0
So 4401-11-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O2/c1-3(5)4-2-6-4/h4H,2H2,1H3
4401-11-0Relevant articles and documents
The Reaction of Dimethyldioxirane with Alkynes
Murray, Robert W.,Singh, Megh
, p. 5076 - 5080 (2007/10/02)
The reaction of dimethyldioxirane with several alkynes gives products which are conveniently rationalized by postulating the intermediacy of oxirenes and oxocarbenes.The latter serve as precursors to H atom or methyl group migration products, as well as to cyclopropane insertion products in some cases.Alkenes, derived from some of these carbene reactions, are partially converted to epoxides.
OXIDATION DE LA METHYL ETHYL CETONE COMPARAISON AVEC L'ACETONE ET LA DIETHYLCETONE
Roux, E. le,Baronnet, F.,Scacchi, G.
, p. 209 - 222 (2007/10/02)
An experimental investigation in a conventional static apparatus of the oxidation of methylethylketone at ca. 350 deg C and subatmospheric pressure confirms the specific features of the reaction, compared with those of the neighbouring ketones, acetone and diethylketone, especially the very long induction period of the first cool flame.To interpret these experimental results, we propose a free radical mechanism based upon the determination of the primary products of the reaction and the evaluation of the rate constants for the elementary steps by the methods of thermochemical kinetics.Contrary to the oxidation reactions of acetone and diethylketone in wich the dominating chain carrier appears to be OH., in the case of methylethylketone HO2. seems to have a key role.It is well known that HO2. cannot be an efficient propagating radical in oxidation reactions and therefore the overall kinetics of the reaction do not trigger off cool flame formation.
