28332-81-2

Usage

Uses

Used in Pharmaceutical Industry:
Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)is employed as a synthetic intermediate for the development of new drugs. Its unique structure allows for the creation of molecules with potential therapeutic applications, making it a valuable asset in the pharmaceutical sector.
Used in Agrochemical Industry:
In the agrochemical field, Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)is utilized as a precursor in the synthesis of biologically active compounds, including potential pesticides. Its role in the development of new agrochemicals is crucial for enhancing crop protection and management strategies.
Used in Research and Development:
Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)is also used as a research compound in the exploration of new chemical entities. Its presence in the scientific community aids in the advancement of knowledge and the discovery of novel applications in both the pharmaceutical and agrochemical industries.

Upstream product

• 618-36-0 rac-methylbenzylamine 
• 407-25-0 trifluoroacetic anhydride 
• 183266-61-7 1-(trifluoroacetyl)benzotriazole 
• 929632-72-4 C₁₇H₁₆F₃NO₃S 
• 354-38-1 2,2,2-trifluoroacetamide 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 383-63-1 ethyl trifluoroacetate, 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 62288-65-7 2,2,2-trifluoro-N-(1-phenylvinyl)acetamide 
• 76-05-1 trifluoroacetic acid 
• 23943-56-8 P,P-diphenyl-N-[(1R)-1-phenylethyl]phosphinic amide 
• 98-86-2 acetophenone 
• 613-91-2 acetophenone oxime 

Downstream Products

• 130632-94-9 (-)-2,2,2-trifluoro-N-(α-methylbenzyl)acetimidoyl chloride 
• 203186-18-9 (S)-2,2,2-trifluoro-N-(1-(4-iodophenyl)ethyl)ethanamide 
• 182141-70-4 N-[(1S)-1-(4-bromophenyl)ethyl]-2,2,2-trifluoroacetamide 
• 447459-97-4 2,2,2-trifluoro-N-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-ethyl}-acetamide 
• 447460-02-8 N-{1-[4-(4-chloro-phenylsulfanyl)-phenyl]-ethyl}-2,2,2-trifluoro-acetamide 
• 864872-82-2 N-[1-(4-benzenesulfonyl-phenyl)-ethyl]-2,2,2-trifluoro-acetamide 
• 864872-83-3 2,2,2-trifluoro-N-{1-[4-(toluene-4-sulfonyl)-phenyl]-ethyl}-acetamide 
• 447460-00-6 N-{1-[4-(4-chlorobenzenesulfonyl)-phenyl]ethyl}-2,2,2-trifluoroacetamide 
• 447460-17-5 N-{1-[4-(4-chloro-2-iodo-benzenesulfonyl)-phenyl]-ethyl}-2,2,2-trifluoro-acetamide 
• 447460-03-9 (S)-1-{4-[4-Chloro-2-(2-fluoro-benzenesulfonyl)-benzenesulfonyl]-phenyl}-ethylamine 
• 447460-30-2 (S)-1-{4-[2-(4-Chloro-benzenesulfonyl)-4-methoxy-benzenesulfonyl]-phenyl}-ethylamine 
• 864872-81-1 2,2,2-trifluoro-N-{1-[4-(4-trifluoromethyl-benzenesulfonyl)-phenyl]-ethyl}-acetamide 

Relevant academic research and scientific papers

Tuning the Circular Dichroism and Circular Polarized Luminescence Intensities of Chiral 2D Hybrid Organic–Inorganic Perovskites through Halogenation of the Organic Ions

Through the incorporation of various halogen-substituted chiral organic cations, the effects of chiral molecules on the chiroptical properties of hybrid organic–inorganic perovskites (HOIPs) are investigated. Among them, the HOIP having a Cl-substituted chiral cation exhibits the highest circular dichroism (CD) and circular polarized luminescence (CPL) intensities, indicating the existence of the largest rotatory strength, whereas the F-substituted HIOP shows the weakest intensities. The observed modulation can be correlated to the varied magnetic transition dipole of HOIPs, which is sensitive to the d-spacing between inorganic layers and the halogen–halogen interaction between organic cations and the inorganic sheets. These counteracting effects meet the optimal CD and CPL intensity with chlorine substitution, rendering the rotatory strength of HOIPs arranged in the order of (ClMBA)2PbI4>(BrMBA)2PbI4>(IMBA)2PbI4>(MBA)2PbI4>(FMBA)2PbI4.

PYRAZOLO-TRIAZINE AND/OR PYRAZOLO-PYRIMIDINE DERIVATIVES AS SELECTIVE INHIBITOR OF CYCLIN DEPENDENT KINASE

The present invention relates to pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[l,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof, the use of these derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferative diseases, inflammatory diseases, immunological diseases, cardiovascular diseases and infectious diseases. Furthermore, the present invention is directed towards pharmaceutical compositions containing at least one of the pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof.

Diastereoselective synthesis of polyfluoroalkylated α-aminophosphonic acid derivatives

The asymmetric synthesis of biorelevant aminophosphonates and aminophosphonic acids bearing trifluoromethyl, tetrafluoroethyl, perfluoropropyl or chlorodifluoromethyl group in the α-position to phosphonyl group is developed. Diastereoselective reduction o

Substituent effects on chiral resolutions of derivatized 1-phenylalkylamines by heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin GC stationary phase

Chiral resolutions of trifluoroacetyl-derivatized 1-phenylalkylamines with different type and position of substituent were investigated by capillary gas chromatography by using heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin diluted in OV-1701 as a chiral stationary phase. The influence of column temperature on retention and enantioselectivity was examined. All enantiomers of meta-substituted analytes as well as fluoro-substituted analytes could be resolved. Temperature had a favorable influence on enantioselectivity for small amines with substituents at the ortho-position. The type of substituent at the stereogenic center of amines also had a crucial effect as the ethyl group led to poor enantioseparation. Among all analytes studied, trifluoroacetyl-derivatized 1-(2′-fluorophenyl)ethylamine exhibited baseline resolution with the shortest analysis time.

Acetic acid as a catalyst for the N-acylation of amines using esters as the acyl source

We report a cheap and simple method for the acetylation of a variety of amines using catalytic acetic acid and either ethyl acetate or butyl acetate as the acyl source. Catalyst loadings as low as 10 mol% afforded acetamide products in excellent yields at temperatures ranging from 80-120 °C. The methodology can also be successfully applied for the synthesis of a broad range of other amides, including the formation of formamides at 20 °C.

Self-Disproportionation of Enantiomers (SDE) via achiral gravity-driven column chromatography of N-fluoroacyl-1-phenylethylamines

The study of the self-disproportionation of enantiomers (SDE) via gravity-driven achiral column chromatography of a series of N-fluoroacetylated amides derived from 1-phenylethylamine is described. The chromatographic experiments performed with N-fluoroacetylated amides confirmed, that the process of molecular association in solution leading to the SDE manifestation, is sensitive to the fluorine content and type of solvent used. Thus, the two opposite eluting profiles for the same compound were observed in two different eluents. Moreover, the amides bearing perfluoroalkyl groups showed opposite eluting order as compared to the established profile for fluorine-free N-acetyl-1-phenylethylamine.

meta-Selective C?H Borylation of Benzylamine-, Phenethylamine-, and Phenylpropylamine-Derived Amides Enabled by a Single Anionic Ligand

Selective functionalization at the meta position of arenes remains a significant challenge. In this work, we demonstrate that a single anionic bipyridine ligand bearing a remote sulfonate group enables selective iridium-catalyzed borylation of a range of common amine-containing aromatic molecules at the arene meta position. We propose that this selectivity is the result of a key hydrogen bonding interaction between the substrate and catalyst. The scope of this meta-selective borylation is demonstrated on amides derived from benzylamines, phenethylamines and phenylpropylamines; amine-containing building blocks of great utility in many applications.

Practical enantioselective hydrogenation of α-aryl- and α-carboxyamidoethylenes by rhodium(I)-{1,2-bis[(o-tert-butoxyphenyl) (phenyl)phosphino]ethane}

The rhodium(I)-{1,2-bis[(o-tert-butoxyphenyl)(phenyl)phosphino]ethane} [Rh(I)-(t-Bu-SMS-Phos)] catalyst system displayed prime efficiency in the hydrogenation of large series of aamidostyrenes and a-amidoacrylates. Up to >99.9% enantiomeric excesses coupl

Transamidation of primary amides with amines catalyzed by zirconocene dichloride

Zirconocene dichloride (Cp2ZrCl2) has been shown to be an effective catalyst for the transamidation of primary amides with amines in cyclohexane at 80°C in 5-24 hours. For favourable substrates, the reaction can be performed at temperatures as low as 30°C.

Transamidation of primary amides with amines catalyzed by zirconocene dichloride

Zirconocene dichloride (Cp2ZrCl2) has been shown to be an effective catalyst for the transamidation of primary amides with amines in cyclohexane at 80°C in 5-24 hours. For favourable substrates, the reaction can be performed at temperatures as low as 30°C.