17257-79-3 Usage
Description
2β-Acetyl-3α-methyloxirane is an organic compound characterized by its unique structure, which features an oxirane ring with a methyl group at the 3α position and an acetyl group at the 2β position. 2β-Acetyl-3α-methyloxirane is known for its potential applications in various fields due to its distinct chemical properties.
Uses
Used in Pharmaceutical Industry:
2β-Acetyl-3α-methyloxirane is used as a starting material for the synthesis of chiral peroxides, which are biologically interesting and may hold clinical importance. These chiral peroxides can be utilized in the development of new drugs and therapeutic agents, contributing to advancements in medicine.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2β-Acetyl-3α-methyloxirane serves as a valuable intermediate for the preparation of various complex organic molecules. Its unique structure allows for selective reactions and functional group transformations, making it a versatile building block in organic chemistry.
Used in Research and Development:
2β-Acetyl-3α-methyloxirane is also used in research and development for studying the properties and reactivity of oxirane-containing compounds. Its synthesis and application in various chemical reactions can provide insights into the behavior of similar molecules, furthering our understanding of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17257-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,5 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17257-79:
(7*1)+(6*7)+(5*2)+(4*5)+(3*7)+(2*7)+(1*9)=123
123 % 10 = 3
So 17257-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2/c1-3(6)5-4(2)7-5/h4-5H,1-2H3
17257-79-3Relevant articles and documents
Iron-Catalyzed Epoxidation of Linear α-Olefins with Hydrogen Peroxide
Mao, Shuxin,Budweg, Svenja,Spannenberg, Anke,Wen, Xiaodong,Yang, Yong,Li, Yong-Wang,Junge, Kathrin,Beller, Matthias
, (2022/01/26)
The combination of Fe(OTf)2 with N-methyl bis(picolylamine) (Me-bpa) L7 enables epoxidation of linear olefins including terminal, internal, and cyclic ones, using hydrogen peroxide as terminal oxidant under mild conditions. In the presence of picolinic acid as additive improved yields of epoxides up to 75 % have been achieved.
Facile epoxidation of α,β-unsaturated ketones with cyclohexylidenebishydroperoxide
Jakka, Kavitha,Liu, Jinyun,Zhao, Cong-Gui
, p. 1395 - 1398 (2007/10/03)
Cyclohexylidenebishydroperoxide was successfully used as the oxygen source for the oxidation of α,β-unsaturated ketones for the first time. The corresponding epoxides were obtained in excellent yields under the Weitz-Scheffer reaction conditions.
TRANSFORMATION OF ACETYLOXIRANES TO THIIRANE ANALOGS
Bubel, O. N.,Tishchenko, I. G.,Stasevich, G. Z.,Veraksich, E. L.,Filich, E. R.
, p. 1082 - 1085 (2007/10/02)
A method for the synthesis of acetylthiiranes was developed; this method includes the conversion of acetyloxiranes to diethylketals, dealkoxylation of the latter, replacement of the oxygen atom of the oxirane ring by sulfur, and acidic hydrolysis of the ethoxyvinylthiirane to acetylthiiranes.
