24503-62-6 Usage
Uses
Used in Pharmaceutical Industry:
3-Chlorotetrafluoropropionyl chloride is utilized as an intermediate in the synthesis of various pharmaceuticals. Its reactivity and ability to form fluorinated compounds make it a valuable component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chlorotetrafluoropropionyl chloride serves as a key intermediate for the production of agrochemicals. Its role in creating fluorinated compounds is essential for enhancing the effectiveness and selectivity of pesticides and other agricultural chemicals.
Used in Specialty Chemicals Manufacturing:
3-Chlorotetrafluoropropionyl chloride is employed as a building block in the synthesis of specialty chemicals. Its unique properties allow for the creation of tailored compounds for specific applications, such as high-performance materials and advanced chemical intermediates.
Used as a Reactive Intermediate:
Due to its strong reactivity, 3-Chlorotetrafluoropropionyl chloride is often used as a reactive intermediate in various chemical reactions. This enables the formation of complex molecules and the development of innovative products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24503-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,0 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24503-62:
(7*2)+(6*4)+(5*5)+(4*0)+(3*3)+(2*6)+(1*2)=86
86 % 10 = 6
So 24503-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C3Cl2F4O/c4-1(10)2(6,7)3(5,8)9
24503-62-6Relevant academic research and scientific papers
Kvicala, J.,Paleta, O.,Dedek, V.
, p. 441 - 457 (1990)
Six chlorofluoropropionyl fluorides were synthesized by converting a -CCl3 group in perhalogenated chlorofluoropropanes to a -COF group in two reaction steps.The ionic telomerization of the acyl fluorides with hexafluoropropene oxide, catalyzed by fluoride ion, afforded mainly a mixture of 1:1 to 1:3 telomers.In some cases, substitution of chlorine for fluorine in the acyl moiety and hexafluoropropene oxide oligomerization occured as side reactions.The effect of the number of chlorines in the starting acyl fluoride on the telomer distribution and by product formation is discussed.The reactivity order of the acyl fluorides Y-COF in the telomerization reaction was: CF3-CClF (2a), CClF2-CF2 (2b) > CF3-CCl2 (3a),CClF2-CClF (3b) > CClF2-CCl2 (4a), CCl2F-CClF (4b).Possible reaction pathways are discussed.
PREPARATION OF 3-CHLOROTETRAFLUOROPROPIONYL CHLORIDE BY CHLORINATION OF THE ESTERS OF 2,2,3,3-TETRAFLUORO-1-PROPANOL
Zabolot-skikh, A. V.,Pozdeeva, V. V.,Zabolot-skikh, V. F.
, p. 1266 - 1268 (2007/10/02)
3-Chlorotetrafluoropropionyl chloride was synthesized by the photochemical chlorination of esters of the alcohol-telomer (n = 1) 2,2,3,3-tetrafluoro-1-propanol followed by thermal decomposition of the obtained α,α-chlorinated esters.
