68295-47-6

Basic information

• Product Name: 2-Pyrrolidinecarboxamide, 5-oxo-N-phenyl-, (2S)-
• CAS NO: 68295-47-6
• Molecular Formula: C11H12N2O2
• Molecular Weight: 204.228
• Mol File: 68295-47-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2-Pyrrolidinecarboxamide, 5-oxo-N-phenyl-, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinecarboxamide, 5-oxo-N-phenyl-, (2S)-(68295-47-6)
• EPA Substance Registry System: 2-Pyrrolidinecarboxamide, 5-oxo-N-phenyl-, (2S)-(68295-47-6)

Safety Data

• Hazardous Substances Data: 68295-47-6(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 4931-66-2 methyl (S)-pyroglutamate 
• 98-79-3 L-Pyroglutamic acid 
• 56-86-0 L-glutamic acid 
• 511543-55-8 (2R,5S)-2-trichloromethyl-1-aza-3-oxabicyclo[3.3.0]octane-4,8-dione 
• 450-99-7 N¹-phenyl-N²-trifluoroacetyl-L-isoglutamine 
• 62121-04-4 N¹-phenyl-L-isoglutamine 

Downstream Products

• 609799-32-8 (2S)-5-oxo-2-(4-bromoanilinocarbonyl)pyrrolidine 
• 1206890-78-9 (S)-5-oxo-N-phenyl-1-((E)-3-phenylacryloyl)pyrrolidine-2-carboxamide 
• 232618-88-1 (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane 
• 609799-33-9 (S)-[(4-bromophenylamino)methyl]pyrrolidine 
• 879899-84-0 N,N-diisopropyl-2-formyl-6-[(2'R,4'S)-2-phenylperhydropyrrolo-(1,2c)-imidazol-3-yl]benzamide 
• 64030-44-0 (2S)-2-(anilinomethyl)pyrrolidine 

Relevant articles and documents

L-Pyroglutamic Sulphonamide as Hydrogen-Bonding Organocatalyst: Enantioselective Diels-Alder Cyclization to Construct Carbazolespirooxindoles

Hydrogen-bonding organocatalysts L-pyroglutamic sulphonamides were readily synthesized for the first time by fully exploiting the potentials of L-pyroglutamic acid. The newly designed catalyst was successfully applied in catalyzing asymmetric Diels-Alder

SMALL MOLECULES AGAINST CEREBLON TO ENHANCE EFFECTOR T CELL FUNCTION

Disclosed are small molecules against cereblon to enhance effector T cell function. Methodos of making thes molecules and methods of using them to treat various disease states are also disclosed.

Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compoun

(S)-5-Oxo-N-phenyl-1-[(E)-3-phenylacryloyl]pyrrolidine-2-carboxamide, easily prepared from inexpensive and readily available, in both enantiomeric forms, glutamic/pyroglutamic acid was designed as an optimal type of chiral Michael acceptor for reactions w