6304-98-9

Basic information

• Product Name: N-[1-oxo-1-(phenylamino)propan-2-yl]benzamide
• CAS NO: 6304-98-9
• Molecular Formula: C₁₆H₁₆N₂O₂
• Molecular Weight: 268.3104
• Mol File: 6304-98-9.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 557.8°C at 760 mmHg
• Flash Point: 222.3°C
• Density: 1.197g/cm³
• Vapor Pressure: 1.78E-12mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: N-[1-oxo-1-(phenylamino)propan-2-yl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[1-oxo-1-(phenylamino)propan-2-yl]benzamide(6304-98-9)
• EPA Substance Registry System: N-[1-oxo-1-(phenylamino)propan-2-yl]benzamide(6304-98-9)

Safety Data

• Hazardous Substances Data: 6304-98-9(Hazardous Substances Data)

Upstream product

• 555-48-6 2-amino-N-phenyl-acetamide 
• 2198-64-3 N-Benzoylalanine 
• 2198-64-3 N-benzoyl-L-alanine 
• 62-53-3 aniline 
• 126727-23-9 <1-(N-tert-butyloxycarbonyl)amino-1-methyl>-N-phenylacetamide 
• 98-88-4 benzoyl chloride 
• 101961-58-4 2-amino-N-phenylpropanamide 
• 65-85-0 benzoic acid 
• 51127-13-0 2-phenyl-4-methyl-4H-oxazolin-5-one 
• 103-72-0 phenyl isothiocyanate 
• 78993-81-4 4-(1-Anilino-1-phenylmethyl)-4-methyl-2-phenyl-2-oxazolin-5-one 
• 397851-05-7 N-Benzoylalanyl chloride 
• 5446-46-8 ethyl 2-(benzoylamino)propanoate 
• 90-02-8 salicylaldehyde 

Downstream Products

• 6304-98-9 (S)-N-benzoyl-alanine anilide 
• 56-41-7 L-alanin 

Relevant articles and documents

A study of the strength of a template molecule - A functional monomer interaction that affects the performance of molecularly imprinted polymers and its application to chiral amplification

A novel type of molecularly imprinted polymer (MIP), N-benzoyl-(S)-valine anilide-imprinted polymer (IP-2), was prepared using hydrogen-bonding interactions as a main force in the pre-polymerization step. The performance of the IP-2 was evaluated via batch procedure and compared with a (S)-valine anilideimprinted polymer (IP-1) that was prepared using an ionic interaction that is stronger than hydrogen bonding. Although both polymers showed a preferential adsorbability for (S)-amino acid derivatives, different performances were observed in terms of adsorbability and enantioselectivity. In addition, the IP-2 was able to recognize the enantiomer of a valine-derived chiral catalyst. This phenomenon was applied to a chiral amplification reaction, and a highly selective asymmetric Mannich-type amination was achieved using the combination of a racemic catalyst and a MIP.

Br?nsted acid catalyzed azlactone ring opening by nucleophiles

Br?nsted acid catalyzed azlactone ring opening in the presence of different nucleophiles leading to the efficient synthesis of protected amides and amino esters is presented. Sixteen compounds were synthesized in good to excellent isolated yields. Mechani

Aminothiazole derivative. I. A convenient synthesis of monocyclic and condensed 5-aminothiazole derivatives

Treatment of diamides derived from α-amino acids with phosphorus pentasulfide or Lawesson's reagent was shown to provide a convenient method to prepare 5-aminothiazoles. By this method, in addition to monocyclic 5-aminothiazoles 19, novel bicyclic 5-aminothiazole derivatives such as 4,5,6,7-tetrahydrothiazolo[5,4-b]pyridines II, 5,6,7,8-tetrahydro-4H-thiazolo[5,4-b]azepines 7, 4,5,6,7,8,9-hexahydrothiazolo[5,4-b]azocine 16 and related compounds were prepared in moderate to good yields from simple diamides, suggesting the wide versatility of the method.