104291-39-6 Usage
Description
4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde is a volatile organic compound (VOC) with the chemical formula C5H3F6O. It is a highly reactive and potentially toxic chemical known for its strong odor. 4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde is commonly used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Uses
Used in Pharmaceutical Industry:
4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties allow for the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical industry, 4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde is utilized as a building block for the creation of novel pesticides and herbicides. Its reactivity enables the production of more effective and targeted agrochemicals.
Used in Specialty Chemicals Industry:
4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde is employed as a versatile intermediate in the synthesis of specialty chemicals, such as fragrances, dyes, and coatings. Its unique properties contribute to the development of innovative and high-performance products.
It is crucial to handle 4,4,4-Trifluoro-3-(trifluoromethyl)crotonaldehyde with caution due to its potential toxicity and strong odor. Proper personal protective equipment and well-ventilated working conditions are essential to ensure the safety of those working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 104291-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,9 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104291-39:
(8*1)+(7*0)+(6*4)+(5*2)+(4*9)+(3*1)+(2*3)+(1*9)=96
96 % 10 = 6
So 104291-39-6 is a valid CAS Registry Number.
104291-39-6Relevant articles and documents
THE REACTION OF SOME 3- AND 4-FLUOROOXETANES WITH ACIDS
Tarrant, Paul,Bull, R. N.
, p. 201 - 216 (1988)
Several oxetanes prepared from hexafluoroacetone and hydrofluoroolefins were treated with aluminum chloride.Substitution of fluorine by chlorine occured on the 3- and 4-carbon atoms as well as cleavage of the ether leakage to give chloroalkyl carbinols or in, some cases, vinyl carbinols.Individual samples of the cis and trans-3,4-difluorooxetanes formed roughly equivalent amounts of the 3-fluoro-4-chlorooxetane stereoisomers, indicating a common carbonium intermediate.Treatment of the 4-fluorooxetane with sulfuric acid gave a dioxetane, a dioxene and an unsaturated aldehyde.
Efforts in Synthesizing α,β-Unsaturated Trifluoromethyl-substituted Aldehydes
Abele, Herbert,Haas, Alois,Lieb, Max
, p. 3502 - 3506 (2007/10/02)
Hexafluoroacetone reacts with ethynylmagnesium bromide to yield (CF3)2C(OH)-CCH (1).Bromine can be added to the triple bond affording the cis/trans-isomer 2.With PCl5 1 yields the allene (CF3)2C=C=CClH (3).The addition of a metalated Schiff base to hexafluoroacetone leads to 4a which on hydrolysis yields (CF3)2C(OH)-CH2-CHO (4b).The reaction of (EtO)2P(O)CH2-R (R = CHO, CO2Et) with hexafluoroacetone gives α,β-unsaturated aldehydes or esters 6. 1,1,1-Trifluoroacetone provides analogous reactions.