74359-10-7 Usage
Uses
Used in Pharmaceutical Industry:
2,2,2-TRIFLUOROETHYL-2-FLUOROACRYLATE is used as a key intermediate for the synthesis of various pharmaceuticals, leveraging its high reactivity to form complex molecular structures that contribute to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,2-TRIFLUOROETHYL-2-FLUOROACRYLATE is utilized as a building block in the creation of novel agrochemicals, enhancing the effectiveness of pesticides and other agricultural products.
Used in Specialty Chemicals Industry:
2,2,2-TRIFLUOROETHYL-2-FLUOROACRYLATE is employed as a reactive component in the production of specialty chemicals, where its ability to participate in multiple chemical reactions allows for the creation of unique and highly specific compounds for various applications.
It is crucial to handle 2,2,2-TRIFLUOROETHYL-2-FLUOROACRYLATE with care due to its potential health hazards if not properly used and stored, emphasizing the need for safety measures during its application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 74359-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74359-10:
(7*7)+(6*4)+(5*3)+(4*5)+(3*9)+(2*1)+(1*0)=137
137 % 10 = 7
So 74359-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F4O2/c1-3(6)4(10)11-2-5(7,8)9/h1-2H2
74359-10-7Relevant articles and documents
REACTIONS OF HALOGEN FLUORIDES XII. REACTION OF BROMINE TRIFLUORIDE WITH BROMINE-CONTAINING ESTERS. A NEW METHOD FOR THE SYNTHESIS OF FLUOROALKYL 2-FLUOROACRYLATES
Kartashov, A. V.,Chuvatkin, N. N.,Boguslavskaya, L. S.
, p. 2243 - 2248 (2007/10/02)
Being weak Lewis bases, esters reduce the reactivity of bromine trifluoride in the substitutive fluorination of organic bromine derivatives.For this reason the rate of the reaction of bromine trifluoride with bromine-containing esters depends not only on the electronic characteristics of the substituents at the reaction center but also on the basicity of the ester.As a rule, the selectivity of the reaction increases with increase in the basicity of the ester.The reaction of bromine trifluoride or chlorine monofluoride with fluoroalkyl 2,3-dibromopropionates can be used successfully for the synthesis of monomers (fluoroalkyl 2-fluoroacrylates).
