24954-62-9

Basic information

• Product Name: Acetamide, N-[2-(4-aminophenyl)ethyl]-2,2,2-trifluoro-
• CAS NO: 24954-62-9
• Molecular Formula: C10H11F3N2O
• Molecular Weight: 232.205
• Mol File: 24954-62-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[2-(4-aminophenyl)ethyl]-2,2,2-trifluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[2-(4-aminophenyl)ethyl]-2,2,2-trifluoro-(24954-62-9)
• EPA Substance Registry System: Acetamide, N-[2-(4-aminophenyl)ethyl]-2,2,2-trifluoro-(24954-62-9)

Safety Data

• Hazardous Substances Data: 24954-62-9(Hazardous Substances Data)

Upstream product

• 13472-00-9 p-Aminophenethylamine 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 168894-49-3 N-(4-(2-((phenylmethyl)amino)ethyl)phenyl)-2-thiophenecarboximidamide 
• 24954-63-0 2,2,2-Trifluoro-N-(2-(4-nitrophenyl)ethyl)acetamide 
• 383-63-1 ethyl trifluoroacetate, 

Downstream Products

• 122842-38-0 2--N,N-dimethyl-2H-benzotriazolyl-5-amine 
• 122854-76-6 N-{2-[4-(5-Dimethylamino-benzotriazol-2-yl)-phenyl]-ethyl}-benzamide 
• 411223-79-5 N-[4-(2-amino-ethyl)-phenyl]-N',N'-dibutyl-N''-(6,7,9,10,12,13,15,16,18,19-decahydro-5,8,11,14,17,20-hexaoxa-benzocyclooctadecen-2-yl)-[1,3,5]triazine-2,4,6-triamine 
• 411223-76-2 1-[4-(2-amino-ethyl)-phenyl]-3-(6,7,9,10,12,13,15,16,18,19-decahydro-5,8,11,14,17,20-hexaoxa-benzocyclooctadecen-2-yl)-urea 
• 101566-04-5 N-<2-<4-<(hydroximinoacetyl)amino>phenyl>ethyl>-2,2,2-trifluoroacetamide 
• 411223-78-4 N-(2-{4-[4-chloro-6-(6,7,9,10,12,13,15,16,18,19-decahydro-5,8,11,14,17,20-hexaoxa-benzocyclooctadecen-2-ylamino)-[1,3,5]triazin-2-ylamino]-phenyl}-ethyl)-2,2,2-trifluoro-acetamide 

Relevant articles and documents

Conjugation of nucleoside triphosphates to an amino linker

A number of nucleoside triphosphates have been linked to a para-aminophenethylamino moiety providing an improved method for the immobilization of nucleotides.

Continuous Synthesis of Aryl Amines from Phenols Utilizing Integrated Packed-Bed Flow Systems

Aryl amines are important pharmaceutical intermediates among other numerous applications. Herein, an environmentally benign route and novel approach to aryl amine synthesis using dehydrative amination of phenols with amines and styrene under continuous-flow conditions was developed. Inexpensive and readily available phenols were efficiently converted into the corresponding aryl amines, with small amounts of easily removable co-products (i.e., H2O and alkanes), in multistep continuous-flow reactors in the presence of heterogeneous Pd catalysts. The high product selectivity and functional-group tolerance of this method allowed aryl amines with diverse functional groups to be selectively obtained in high yields over a continuous operation time of one week.

Acylaminoalkyl-substituted benzenesulfonamide derivatives, their preparation, their use and pharmaceutical preparations comprising them

One embodiment of the present invention relates to acylaminoalkyl-substituted benzenesulfonamide derivatives of the formula (I), 1in which A, R(1), R(2), X, Y, and Z have the meanings indicated in the specification, and to pharmaceutically tolerable salt