374-41-4 Usage
Uses
Used in Chemical Synthesis:
3,3,4,4,4-Pentafluorobutan-2-one is used as a solvent for various chemical reactions due to its unique properties, facilitating the process and improving the efficiency of synthesis.
Used in Fluorinated Compounds Production:
As a precursor, 3,3,4,4,4-Pentafluorobutan-2-one is instrumental in the production of other fluorinated compounds, which are essential in a range of applications across different industries.
Used in Pharmaceutical Synthesis:
3,3,4,4,4-Pentafluorobutan-2-one is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 3,3,4,4,4-Pentafluorobutan-2-one serves as a vital component in the synthesis of various agrochemicals, enhancing crop protection and yield.
Used in Plastics and Polymers Manufacturing:
3,3,4,4,4-Pentafluorobutan-2-one is utilized in the manufacturing process of plastics and polymers, where its properties contribute to the creation of materials with specific characteristics required for various applications.
Used in Electronics Industry:
3,3,4,4,4-PENTAFLUOROBUTAN-2-ONE finds use in the electronics industry, particularly in the production of certain types of electronic components, where its properties are beneficial for performance and reliability.
Check Digit Verification of cas no
The CAS Registry Mumber 374-41-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 374-41:
(5*3)+(4*7)+(3*4)+(2*4)+(1*1)=64
64 % 10 = 4
So 374-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F5O/c1-2(10)3(5,6)4(7,8)9/h1H3
374-41-4Relevant academic research and scientific papers
(Z) -Trifluoromethyl-Trisubstituted Alkenes or Isoxazolines: Divergent Pathways from the Same Allene
Liu, Chaolun,Rowland, Casey A.,Tius, Marcus A.,Yap, Glenn P. A.
supporting information, p. 7208 - 7212 (2020/10/02)
Because of a charge-dipole interaction involving nonbonding electron pairs on fluorine, protonation of trifluoromethyl allenes leads to tri- or tetrasubstituted alkenes with high (Z)-selectivity. Treatment of the same allenes with catalytic Au(I) initiates a reaction cascade that produces isoxazolines in high yield.
2,2-Dihydroperfluoropentane (HFC 4310 mf) synthesis from HFP dimer
Cheburkov, Yuri,Moore, George G.I.
, p. 227 - 231 (2007/10/03)
The thermodynamic dimer of hexafluoropropene (HFP) may be used for the one pot synthesis of 2H-perfluoro-2-pentene, which is the starting compound for preparation of 2,2-dihydroperfluoropentane (HFC 4310 mf).
