407-37-4 Usage
Uses
Used in Chemical Synthesis:
AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new and improved products in these industries.
Used in Organic Chemistry:
AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)serves as a reagent in organic chemistry reactions, facilitating specific transformations and reactions that are essential for the synthesis of complex organic molecules.
Used in Solvent Applications:
AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)is employed as a solvent in various industrial processes, leveraging its chemical properties to dissolve a range of substances and support chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)is used as a building block for the creation of new drugs, potentially leading to advancements in medicinal chemistry and therapeutics.
Used in Agrochemical Industry:
Similarly, in agrochemicals, AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)- is used to develop new pesticides or herbicides, enhancing agricultural productivity and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 407-37-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 407-37:
(5*4)+(4*0)+(3*7)+(2*3)+(1*7)=54
54 % 10 = 4
So 407-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F6NO/c5-3(6,7)1-11-2(12)4(8,9)10/h1H2,(H,11,12)
407-37-4Relevant academic research and scientific papers
Romanov,Vasil'ev,Zatonsky
, p. 1639 - 1644 (2001)
N-Substituted trifluoroacetimidoyl halides in ionic-type transformations readily undergo nucleophilic substitution and dehydrofluorination rather than 1,3-dehydrohalogenation to give nitrile ylides.
Sigmatropic isomerizations in azaallyl systems: XXII. 1,3-proton transfer in (N-alkyltrifluoroacetimidoyl)phosphonates
Onys'ko,Kim,Kiseleva,Pustovit,Sinitsa
, p. 1197 - 1203 (2008/02/03)
The reaction of N-alkyltrifluoroacetimidoyl chlorides with trialkyl phosphites leads to corresponding imidoylphosphonates CF 3C[P(O)(OAlk)2]=NCH2R. These compounds undergo irreversible 1,3-H shift catalyzed by nitrogenous bases to give phosphorylated imines CF3CH[P(O)(OAlk)2]N=CHR. The tendency for prototropism increases with increasing electronegativity of substituents R: CF3 > CH2OMe > H > Me. N-Cyclopentyl analogs of the obtained compounds show no tendency for prototropism. Imidoylphosphonates exist mainly as Z isomers [Z/E (6-10) : 1].
