5829-03-8 Usage
Uses
Used in Agrochemical Production:
ETHYL 2-CHLOROTETRAFLUOROPROPIONATE is used as an intermediate in the production of agrochemicals, contributing to the development of various pesticides and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Used in Pharmaceutical Production:
In the pharmaceutical industry, ETHYL 2-CHLOROTETRAFLUOROPROPIONATE serves as an intermediate for the synthesis of different medicinal compounds. Its unique properties as a fluorinated ester make it a valuable component in the creation of new drugs with specific therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5829-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5829-03:
(6*5)+(5*8)+(4*2)+(3*9)+(2*0)+(1*3)=108
108 % 10 = 8
So 5829-03-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClF4O2/c1-2-12-3(11)4(6,7)5(8,9)10/h2H2,1H3
5829-03-8Relevant academic research and scientific papers
REACTIONS OF CHLORINE MONOFLUORIDE. IV. ADDITION OF CHLORINE MONOFLUORIDE TO HALOGEN-SUBSTITUTED ALKENES
Boguslavskaya, L. S.,Chuvatkin, N. N.,Panteleeva, I. Yu.
, p. 1832 - 1842 (2007/10/02)
The reactions of chlorine monofluoride with halogenoethylenes (1,1-dichloro-, 1,2-dichloro-, trichloro-, and tetrachloroethylenes) and halogenopropenes ( 3-bromo-, 3,3,3-trichloro-, E- and Z-1,3-dichloro-, 3-chloro-2-methyl-, and perfluoropropenes) were investigated in inert solvents in the presence of ethyl acetate as external nucleophile.In all cases chloroacyloxy adducts were isolated and identified in addition to the chlorofluorination products, and this indicates an electrophilic mechanism for the chlorofluorination of polyhalogenoalkenes.Methyl chloromaleate, chlorofumarate, chlorofluoroethylenedicarboxylate, α,β-difluoroacrylate, and perfluoromethacrylate in anhydrous hydrogen fluoride form the corresponding chlorofluoro adducts with satisfactory yields, whereas the reaction takes place with difficulty in inert solvents.
