5930-66-5 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Chlorotetrafluoropropionyl fluoride is utilized as an intermediate in the production of pharmaceuticals, contributing to the development of new medications and enhancing the properties of existing ones.
Used in Agrochemical Production:
In the agrochemical industry, 3-CHLOROTETRAFLUOROPROPIONYL FLUORIDE serves as a key intermediate, aiding in the synthesis of various agrochemicals that are essential for crop protection and enhancement of agricultural yields.
Used in Fine Chemicals Synthesis:
3-Chlorotetrafluoropropionyl fluoride is employed in the synthesis of fine chemicals, which are high-purity, specialty chemicals used in various applications, including research, diagnostics, and high-value industrial processes.
Used in Fluorinated Compounds Production:
As a building block, 3-CHLOROTETRAFLUOROPROPIONYL FLUORIDE is instrumental in the creation of fluorinated compounds, which have a wide range of applications due to their unique properties, such as increased stability and reactivity.
Used as a Solvent in Organic Synthesis:
3-Chlorotetrafluoropropionyl fluoride functions as a solvent in organic synthesis, facilitating various chemical reactions and improving the efficiency of synthesis processes.
Used as a Reagent in Fluorination Reactions:
3-CHLOROTETRAFLUOROPROPIONYL FLUORIDE is also used as a reagent in fluorination reactions, where it helps to introduce fluorine atoms into target molecules, enhancing their properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 5930-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5930-66:
(6*5)+(5*9)+(4*3)+(3*0)+(2*6)+(1*6)=105
105 % 10 = 5
So 5930-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C3ClF5O/c4-3(8,9)2(6,7)1(5)10
5930-66-5Relevant academic research and scientific papers
HALOGEN FLUOROSULFATE REACTIONS WITH FLUOROCARBONS
Shack, Carl J.,Christe, K. O.
, p. 63 - 74 (2007/10/02)
The scope of the reaction of simple fluorocarbon halides with chlorine fluorosulfate and mixtures of chlorine and bromine fluorosulfate to produce RfOSO2F compounds has been investigated.It is shown that in many cases even primary chlorine in -CF2Cl groups can be replaced by -OSO2F.Primary bromine or iodine in -CF2X are more readily replaced.The mechanism of this replacement reaction has been established by the isolation of the metastable iodine III intermediate RfI(OSO2F)2.Neither secondary chlorine nor bromine in -CFX- groups is affected.With the secondary iodide, i-C3F7I, the salt + - is formed.Furthermore, it has been found that ClOSO2F is capable of converting fluorocarbon acids or their derivatives into fluorocarbon halides.A combination of these two ClOSO2F reactions with the known conversion of RfCF2OSO2F to the corresponding fluorocarbon acid offers a novel, high yield chain shortening reaction for the otherwise unreactive fluorocarbon halides according to:
