33558-02-0

Basic information

• Product Name: L-Phenylalanine, N-[(phenylamino)carbonyl]-
• CAS NO: 33558-02-0
• Molecular Formula: C16H16N2O3
• Molecular Weight: 284.315
• Mol File: 33558-02-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[(phenylamino)carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[(phenylamino)carbonyl]-(33558-02-0)
• EPA Substance Registry System: L-Phenylalanine, N-[(phenylamino)carbonyl]-(33558-02-0)

Safety Data

• Hazardous Substances Data: 33558-02-0(Hazardous Substances Data)

Upstream product

• 65-85-0 benzoic acid 
• 63-91-2 L-phenylalanine 
• 86298-24-0 N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide 
• 103-71-9 phenyl isocyanate 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 138088-28-5 (S)-3-phenyl-2-(3-phenyl-ureido)-propionic acid methyl ester 
• 673-06-3 D-(R)-phenylalanine 
• 2221-08-1 3-phenyl-5-benzyl-hydantoin 

Downstream Products

• 33557-82-3 2-(1-Nitroso-3-phenylureido)-3-phenylpropionsaeure 

Relevant articles and documents

One-pot preparation of carbamoyl benzotriazoles and their applications in the preparation of ureas, hydrazinecarboxamides and carbamic esters

Carbamoyl benzotriazoles were conveniently synthesized in one-pot from carboxylic acids, diphenyl phosphorazidate (DPPA) and 1H-benzotriazole (BtH). The reactivity and applications of carbamoyl benzotriazoles were also explored. Carbamoyl benzotriazoles react smoothly with amino acids, hydrazines and alcohols, thus providing facile access to the corresponding ureas, hydrazinecarboxamides and carbamic esters, respectively, in good to excellent yields.

Carboxamide derivatives and their use in the treatment of thromboembolic diseases and tumours

Compounds of the formula (I), in which the variables have the following meaning, D is phenyl or pyridyl, each of which is unsubstituted or monosubstituted or polysubstituted by Hal, A, OR2, N(R2)2, NO2, CN, COOR