431-32-3 Usage
Uses
Used in Pharmaceutical Industry:
2,3,3,3-TETRAFLUOROPROPIONITRILE is used as a chemical intermediate for the production of pharmaceuticals, contributing to the development of new drugs and enhancing the efficacy of existing medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3,3,3-TETRAFLUOROPROPIONITRILE serves as a key intermediate, playing a crucial role in the synthesis of agrochemicals that help protect crops and improve agricultural productivity.
Used in Specialty Chemicals Production:
2,3,3,3-TETRAFLUOROPROPIONITRILE is employed as an intermediate in the creation of specialty chemicals, which are used in a wide range of applications, from coatings and adhesives to high-performance materials.
Used as a Solvent:
2,3,3,3-TETRAFLUOROPROPIONITRILE also functions as a solvent in various chemical processes, facilitating reactions and improving the efficiency of chemical synthesis.
Safety Precautions:
Given its toxic nature if ingested or inhaled, and the potential for skin and eye irritation, 2,3,3,3-TETRAFLUOROPROPIONITRILE requires careful handling and storage. Proper safety measures should be implemented to prevent accidents and minimize harmful effects on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 431-32-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 431-32:
(5*4)+(4*3)+(3*1)+(2*3)+(1*2)=43
43 % 10 = 3
So 431-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C3HF4N/c4-2(1-8)3(5,6)7/h2H
431-32-3Relevant articles and documents
IONIC DIMERISATION OF TRIFLUOROPROPENENITRILE AND ITS ADDITION REACTIONS WITH METHYL TRIFLUOROPROPENOATE
Svoboda, Jiri,Paleta, Oldrich,Dedek, Vaclav
, p. 406 - 414 (2007/10/02)
Dimerisation of trifluoropropenenitrile (I) in the presence of potassium fluoride and tertiary amines afforded a mixture of stereoisomeric perfluoro-4-methyl-2-pentenedinitriles (II), higherboiling compounds, and 2,3,3,3-tetrafluoropropanenitrile (III) which arises by proton transfer from the solvent molecule.Under optimum conditions, product II was obtained in about 50percent yield.Reaction of the nitrile I with methyl trifluoropropenoate (IV) gave, besides the dimers II and V, the product of addition of the nitrile I to the propenoate, IV, i.e. methyl 4-cyanoperfluoro-2-pentenoate (VI), and the addition product of the propenoate IV to the nitrile I, i.e. methyl 4-cyanoperfluoro-2-methyl-3-butenoate (VII).The relative reactivity of I and IV is discussed.The ratio of stereoisomers in II, V, VI and VII indicates that the magnitude of the steric substituent effect, operating in the reaction mechanism, decreases in the order -CFCF3(COOCH3)> -CFCF3(CN)> -COOCH3> -CN.
