68464-36-8

Upstream product

• 815-06-5 N-methyl-2,2,2-trifluoroacetamide 
• 100-39-0 benzyl bromide 
• 103-67-3 benzyl-methyl-amine 
• 407-25-0 trifluoroacetic anhydride 
• 7387-69-1 N-benzyl-2,2,2-trifluoroacetamide 
• 74-88-4 methyl iodide 
• 5672-89-9 N-trifluoroacetoxy succinimide 
• 100-46-9 benzylamine 
• 100-44-7 benzyl chloride 
• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 

Downstream Products

• 122982-83-6 Benzyl-((E)-3-cyclohexyl-1-trifluoromethyl-propenyl)-methyl-amine 
• 122982-82-5 Benzyl-((Z)-3-cyclohexyl-1-trifluoromethyl-propenyl)-methyl-amine 
• 122982-82-5 Benzyl-((E)-3-cyclohexyl-1-trifluoromethyl-propenyl)-methyl-amine 
• 122982-85-8 (E) 1,1,1-Trifluoro-2-methyl-benzylamino-5-phenyl-2-pentene 
• 122982-84-7 (Z) 1,1,1-Trifluoro-2-methyl-benzylamino-5-phenyl-2-pentene 
• 122982-84-7 1,1,1-Trifluoro-2-methyl-benzylamino-5-phenyl-2-pentene 
• 122982-81-4 Benzyl-methyl-((E)-1-trifluoromethyl-oct-1-enyl)-amine 
• 122982-80-3 Benzyl-methyl-((Z)-1-trifluoromethyl-oct-1-enyl)-amine 
• 122982-80-3 Benzyl-methyl-((E)-1-trifluoromethyl-oct-1-enyl)-amine 
• 103-67-3 benzyl-methyl-amine 
• 379-18-0 1,1-diphenyl-2,2,2-trifluoroethanol 
• 122983-01-1 N-benzyl-1,1,1-trifluoro-N-methyl-5-phenylpentan-2-amine 
• 122982-91-6 1,1,1-Trifluoro-2-methylbenzylamino-5-phenyl-2-pentene hydrochloride 
• 1329562-78-8 N-(4-hexylbenzyl)-N-methyltrifluoroacetamide 

Relevant academic research and scientific papers

AN EXPERIMENTAL STUDY OF SOME NMR METHODS FOR THE MEASUREMENT OF SLOW EXCHANGE RATES

The rate of interconversion of the cis and trans rotational isomers of N-triflouroacetyl-N-methylbenzylamine have been determined by a variety of NMR lineshape experiments and by several double resonance methods.Comparison of the results for the slow exch

Electrochemical approach to trifluoroacetamide synthesis from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) catalyzed by B12complex

One-pot synthetic approach to produce trifluoroacetamide has been developed using an electrochemical method with the B12 complex as a catalyst under mild conditions, in open air at room temperature. Thirty examples of trifluoroacetamide were synthesized from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) in moderate to good yields. This user-friendly strategy is compatible with a broad range of trifluoroacetamide syntheses.

Fabrication of asymmetric molecular junctions by the oriented assembly of dithiocarbamate rectifiers

The oriented assembly of molecules on metals is a requirement for rectification in planar metal-molecule-metal junctions. Here, we demonstrate how the difference in adsorption kinetics between dithiocarbamate and thioacetate anchor groups can be utilized

THIENOPYRIMIDONE COMPOUND

The present invention relates to a compound represented by the formula: wherein Ar is an optionally substituted ring; A is a spacer having a main chain of 1 to 4 atoms; B is a bond, a C1-10 alkylene group or an oxygen atom; R3 and R5 are each independently a hydrogen atom or a substituent; R4 is an optionally substituted cyclic group or an optionally substituted C1-10 alkyl group; and R1 and R2 are each independently a hydrogen atom or a substituent, or R1 and R2 or R1 and B are bonded to form an optionally substituted nitrogen-containing heterocycle, or R1 and Ar are bonded to form an optionally substituted nitrogen-containing fused heterocycle, or a salt thereof. The thienopyrimidone compound of the present invention has a superior melanin-concentrating hormone receptor antagonistic action, and is useful as an agent for the prophylaxis or treatment of obesity and the like.

A CONVENIENT SYNTHESIS OF N-ALKYL AND N,N-DIALKYLTRIFLUOROACETAMIDES IN A SOLID-LIQUID TWO-PHASE SYSTEM IN THE PRESENCE OF PHASE-TRANSFER CATALYSTS

Trifluoroacetamide is easily monoalkylated in a K2CO3-organic solvent solid-liquid two-phase system affording in good to excellent yields N-alkyltrifluoroacetamides.Under the same conditions, the latter, in turn, ract with alkylating agents giving N,N-dialkyltrifluoroacetamides in high yields.