1422-36-2 Usage
Uses
Used in Organic Synthesis:
5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE, 97% MIN. is used as a building block in organic synthesis for creating complex organic molecules. Its unique structure and high purity make it a valuable component in the synthesis of various compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE, 97% MIN. is used as an intermediate in the production of pharmaceuticals. Its reactive nature and specific structure allow it to be incorporated into the synthesis of various drug molecules, contributing to the development of new medications.
Used in Agrochemical Industry:
5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE, 97% MIN. is also used in the agrochemical industry as a precursor for the synthesis of agrochemicals. Its unique properties make it suitable for the development of new pesticides and other agricultural chemicals.
Used as a Reagent in Chemical Reactions:
Due to its reactive nature, 5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE, 97% MIN. is used as a reagent in various chemical reactions. Its specific structure allows it to participate in a range of reactions, making it a versatile component in the synthesis of different compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1422-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1422-36:
(6*1)+(5*4)+(4*2)+(3*2)+(2*3)+(1*6)=52
52 % 10 = 2
So 1422-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F6O/c1-3(13)2-4(5(7,8)9)6(10,11)12/h2H,1H3
1422-36-2Relevant academic research and scientific papers
Synthesis and photosynthetic inhibition activity of substituted 5-(bis-trifluoromethyl)methyl)-2-aminothiazoles
Boyer, Cécile,Finazzi, Giovanni,Laurent, Philippe,Haas, Alois,Blancou, Hubert
, p. 1522 - 1527 (2008/09/16)
The reaction of 5,5,5-trifluoro-4-trifluoromethyl-pent-3-en-2-one with aminothiocarbonyls yielded aminothiourea precursors which readily cyclised to the corresponding thiazole derivatives, 5-(bis-trifluoromethyl)methyl)-2-aminothiazoles. The inhibitory po
Preparation of Suitable Precursors for the Synthesis of 16,16,16,17,17,17-Hexafluororetinals
Abele, Herbert,Haas, Alois,Lieb, Max,Zwingenberger, Joerg
, p. 145 - 150 (2007/10/02)
Cycloaddition reactions of (CF3)2C=CHCHO with butadiene or 1,3-pentadiene provide the corresponding cyclohexane derivatives 2, 3 and 4.Condensation of 3 with (C2H5O)2P(O)CH2C(O)CH3 or of 2 with acetone in the presence of bases yields 5 and 7.While 5 react
