4510-37-6 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(2,3-dimethyloxiranyl)is used as a building block in organic synthesis for its ability to participate in a range of chemical reactions. Its presence in the synthesis of complex organic molecules is attributed to its reactivity and the stability it provides to the molecular structures formed.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethanone, 1-(2,3-dimethyloxiranyl)is utilized as an intermediate in the production of various pharmaceutical compounds. Its unique structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Chemical Industry:
Ethanone, 1-(2,3-dimethyloxiranyl)is also used in the chemical industry for the development of specialty chemicals, such as solvents, coatings, and adhesives. Its versatility in reactions and compatibility with a wide range of other chemicals make it a valuable asset in the formulation of these products.
Safety Considerations:
It is important to handle Ethanone, 1-(2,3-dimethyloxiranyl)with care due to its potential flammability and harmful effects if ingested or inhaled. Proper safety measures, including the use of protective equipment and adherence to safety protocols, are essential when working with Ethanone, 1-(2,3-dimethyloxiranyl)-.
Check Digit Verification of cas no
The CAS Registry Mumber 4510-37-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4510-37:
(6*4)+(5*5)+(4*1)+(3*0)+(2*3)+(1*7)=66
66 % 10 = 6
So 4510-37-6 is a valid CAS Registry Number.
4510-37-6Relevant academic research and scientific papers
Polymer-supported Oxone and tert-butyl hydroperoxide: new reagents for the epoxidation of α,β-unsaturated aldehydes and ketones
Pourali, Ali Reza
experimental part, p. 113 - 115 (2010/06/19)
Efficient, mild and selective epoxidation of α,β-unsaturated aldehydes and ketones was performed using polyvinylpyrrolidonesupported Oxone (Oxone/PVP) and ButOOH/PVP.
REACTION OF ACETYLOXIRANES WITH ACETONITRILE
Bubel', O. N.,Tishchenko, I. G.,Ptashnikov, Yu. L.
, p. 773 - 775 (2007/10/02)
2-Acetyloxiranes react with acetonitrile in the presence of equimolar amounts of Lewis acids.It was established that the use of boron trifluoride etherate or sulfuric acid as the catalyst leads to 2,7- and 3,6-diepoxy-1,5-dioxocanes, the use of aluminum trichloride, as well as stannic chloride, leads to the corresponding chlorohydrins, while the use of gaseous boron trifluoride leads to 2-oxazolines in satisfactory yields.It is shown that the reaction is regio- and stereospecific and that the resulting substituted 2-methyl-5-acetyl-2-oxazolines have a cis configuration.
SYNTHESIS OF 2-ALKYLTHIO-5-ACETYL-2-OXAZOLINES
Bubel', O.N.,Tishchenko, I.G.,Grinkevich, O.A.,Abramov, A.F.
, p. 352 - 355 (2007/10/02)
The reaction of 2-acetyloxiranes with alkyl thiocyanates in the presence of Lewis acids (BF3, AlCl3) has given 2-alkylthio-5-acetyl-2-oxazolines (yields 40-60percent).It has been shown that the reaction of trans-2-acetyl-3-methyloxirane and of trans-2-acetyl-3-methyloxirane and of trans-2-acetyl-2,3-dimethyloxirane with alkyl thiocyanates takes place stereospecifically and leads to cis-2-alkylthio-5-acetyl-2-oxazolines.
