814-79-9 Usage
Uses
Used in Pharmaceutical Industry:
3-Fluoro-2-butanone is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones.
Used in Organic Compounds Synthesis:
It is utilized as a key component in the production of a range of organic compounds, enhancing the diversity and complexity of chemical products available for various applications.
Used as a Solvent:
3-Fluoro-2-butanone is employed as a solvent in various chemical processes, facilitating reactions and improving the efficiency of industrial operations.
Used in Flavor and Fragrance Industry:
It is used as a component in the manufacturing of flavor and fragrance products, adding to the richness and variety of scents and tastes in consumer goods.
Safety Considerations:
Given its highly flammable properties, 3-Fluoro-2-butanone requires strict adherence to safety protocols and guidelines during handling, storage, and use to prevent accidents and ensure the safety of personnel and equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 814-79-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 814-79:
(5*8)+(4*1)+(3*4)+(2*7)+(1*9)=79
79 % 10 = 9
So 814-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H7FO/c1-3(5)4(2)6/h3H,1-2H3
814-79-9Relevant academic research and scientific papers
Halogen Epoxides, 3. Reactions of 2-Chloro- and 2,3-Dichlorooxiranes with Silver Tetrafluoroborate: Synthesis of α-Fluorinated Carbonyl Compounds
Griesbaum, Karl,Keul, Helmut,Kibar, Riza,Pfeffer, Bernd,Spraul, Manfred
, p. 1858 - 1870 (2007/10/02)
Reactions of chlorinated oxiranes with silver tetrafluoroborate in ether have been investigated.Substituted-2-chlorooxiranes (4a - e) afforded the corresponding α-fluorocarbonyl compounds (7a - e) as major products and the isomeric α-chlorocarbonyl compounds (8a - e) as minor products.Substituted 2,3-dichlorooxiranes (10, 14, 20, 24) yielded the isomeric α,α-dichloroketones (13, 19, 22, 26b, 29b) as well as the corresponding α-chloro-α-fluoroketones (12, 17, 21, 26a, 29a) and α,β-unsaturated α-chloroketones (18, 23, 27, 30).The course of the reaction was rationalized.Similar reaction with α-chloroketones and with α,α-dichloroketones succeeded only at substrates (8b, 35) in which the chlorine substituents were in benzylic positions.
