406-95-1 Usage
Description
2,2,2-Trifluoroethyl acetate is an organic compound that features a trifluoromethyl group attached to an ethyl acetate moiety. It is known for its unique chemical properties, which make it a versatile building block in the synthesis of various pharmaceuticals and chemical compounds.
Uses
Used in Pharmaceutical Industry:
2,2,2-Trifluoroethyl acetate is used as a synthetic intermediate for the preparation of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs with improved properties, such as enhanced bioavailability and selectivity.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,2,2-Trifluoroethyl acetate is used as a key building block for the creation of a wide range of chemical compounds. Its trifluoromethyl group imparts specific characteristics to the final products, making it valuable in the development of new materials with tailored properties.
Specific Application:
2,2,2-Trifluoroethyl trifluoroacetate, a derivative of 2,2,2-trifluoroethyl acetate, is used in the preparation of dimethyl (3,3,3-trifluoro-2,2-dihydroxypropyl)phosphonate. 2,2,2-TRIFLUOROETHYL ACETATE has potential applications in the development of new pharmaceuticals and other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 406-95-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 406-95:
(5*4)+(4*0)+(3*6)+(2*9)+(1*5)=61
61 % 10 = 1
So 406-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H5F3O2/c1-3(8)9-2-4(5,6)7/h2H2,1H3
406-95-1Relevant articles and documents
Imidazolium salt assisted hydrolysis of 1-chloro-2,2,2-trifluoroethane
Lee, Hyunjoo,Kim, Kyung Hwan,Kim, Honggon,Lee, Sang Deuk,Kim, Hoon Sik
, p. 95 - 98 (2004)
The use of imidazolium-based ionic liquids as promoters was found to be highly effective for the hydrolysis reaction of CF3CH2Cl with aqueous potassium acetate to produce 2,2,2-trifluoroethanol (TFE). Among ionic liquids tested, 1-butyl-3-methylimidazoliu
EFFECT OF SOLVENT ON THE ESTERIFICATION BETWEEN 1,1,1-TRIFLUOROCHLORETHANE AND AKALINE ACETATE
Shibuta, Daisuke,Watanabe, Masanari,Sato, Kosei
, p. 176 (1985)
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BF3·2CF3CH2OH (BF 3·2TFE), an efficient superacidic catalyst for some organic synthetic transformations
Prakash, G. K. Surya,Mathew, Thomas,Marinez, Eric R.,Esteves, Pierre M.,Rasul, Golam,Olah, George A.
, p. 3952 - 3958 (2007/10/03)
BF3 · 2CF3CH2OH complex was found to be a very effective superacidic catalyst comparable in acid strength to at least that of 100% anhydrous sulfuric acid for various acid-catalyzed organic transformations such as isomerizations, rearrangements, ionic hydrogenation of various ketones, and aromatics with triethylsilane and nitration of aromatics with metal nitrate. Studies of the pivalaldehyde-methyl isopropyl ketone rearrangement and the benzopinacol to phenanthrene transformation suggest that the complex has an acidity comparable to that of 100% anhydrous sulfuric acid. The structure and properties of the 1:2 boron trifluoride-trifluoroethanol complex have been further studied using NMR (1H, 13C, 19F, 11B) and DFT calculations at the B3LYP/6- 311++G**//B3LYP/6-31G* level.