24003-71-2

Basic information

• Product Name: (2S)-phenyl[(phenylacetyl)amino]ethanoic acid
• CAS NO: 24003-71-2
• Molecular Formula: C₁₆H₁₅NO₃
• Molecular Weight: 269.2952
• Mol File: 24003-71-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 533.3°C at 760 mmHg
• Flash Point: 276.3°C
• Density: 1.239g/cm³
• Vapor Pressure: 3.33E-12mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: (2S)-phenyl[(phenylacetyl)amino]ethanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-phenyl[(phenylacetyl)amino]ethanoic acid(24003-71-2)
• EPA Substance Registry System: (2S)-phenyl[(phenylacetyl)amino]ethanoic acid(24003-71-2)

Safety Data

• Hazardous Substances Data: 24003-71-2(Hazardous Substances Data)

Upstream product

• 56674-25-0 2-hydroxy-2-(2-phenylacetamido)acetic acid 
• 71-43-2 benzene 
• 103-81-1 Benzeneacetamide 
• 2835-06-5 phenylglycin 
• 103-80-0 phenylacetyl chloride 
• 24461-61-8 phenylglycine methyl ester 
• 171181-53-6 methyl N^α-(diphenylmethylene)-DL-phenylglycinate 

Downstream Products

• 63069-08-9 N-(3-cyclohexyl-2-cyclohexylimino-4-oxo-5-phenyl-oxazolidin-5-yl)-2-phenyl-acetamide 

Relevant articles and documents

GRANZYME B DIRECTED IMAGING AND THERAPY

Provided herein are heterocyclic compounds useful for imaging Granzyme B. Methods of imaging Granzyme B, combination therapies, and kits comprising the Granzyme B imaging agents are also provided.

Regioselective synthesis of tetrasubstituted pyrroles by 1,3-dipolar cycloaddition and spontaneous decarboxylation

We developed a novel regioselective synthesis of tetrasubstituted pyrroles via the classic 1,3-dipolar cycloaddition of α,β-unsaturated benzofuran-3(2H)-one and azlactones (1) followed by spontaneous decarboxylation. The complete regiochemical control of tetrasubstituted pyrroles was confirmed by the orthogonal synthesis of complementary regioisomers (7a and 7b) simply by using different azlactones (1a and 1b, respectively).

INTER VS INTRAMOLECULAR AMIDOALKYLATIONS OF AROMATICS - A NEW SYNTHESIS OF OXINDOLES, ISOQUINOLONES AND BENZAZEPINONES

A new synthesis of oxindoles (8) isoquinolones (5) and benzazepinones (10) by the intramolecular amidoalkylation of aromatic amides of bismethoxycarbonylaminoacetic acid (4, 7, 9) is described.