197007-02-6

Basic information

• Product Name: ethyl 3-(N-phenylamino)-2-phenylpropenoate
• Synonyms: ethyl 3-(N-phenylamino)-2-phenylpropenoate
• CAS NO: 197007-02-6
• Molecular Weight: 267.327
• Mol File: 197007-02-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: ethyl 3-(N-phenylamino)-2-phenylpropenoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-(N-phenylamino)-2-phenylpropenoate(197007-02-6)
• EPA Substance Registry System: ethyl 3-(N-phenylamino)-2-phenylpropenoate(197007-02-6)

Safety Data

• Hazardous Substances Data: 197007-02-6(Hazardous Substances Data)

Upstream product

• 908094-04-2 phenyldiazomethane 
• 623-73-4 diazoacetic acid ethyl ester 
• 538-51-2 benzylidene phenylamine 
• 62-53-3 aniline 
• 100-52-7 benzaldehyde 
• 20414-50-0 ethyl trans-1,3-diphenylaziridine-2-carboxylate 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 67-56-1 methanol 

Downstream Products

• 25410-99-5 3-phenylquinolin-4(1H)-one 

Relevant articles and documents

Synthesis of asymmetric iron-pybox complexes and their application to aziridine forming reactions

The synthesis of a series of iron-pybox complexes and their employment in the catalytic asymmetric aziridine forming reaction is presented. When AgSbF6 is used as an initiator, the i-pr- and t-bu-pybox complexes produce 47% of the cis-aziridine

Pharmaceutical compositions comprising 4-quinolones for treating cancers

A non-cytotoxic pharmaceutical composition acting on the proliferation of clonogenic cells in malignant tumors and including an efficient amount of a compound selected among the compounds of formula (I) and (Ia).

InCl3 catalyzed reactions of ethyl diazoacetate with aldimines: A highly diastereoselective synthesis of cis-aziridine carboxylates

InCl3 catalyzed reactions of ethyl diazoacetate with aldimines give aziridine carboxylates under mild conditions, low catalyst loading and with high cis-selectivity. (C) 2000 Elsevier Science Ltd.