76862-09-4

Basic information

• Product Name: Glycine, N-[(4-chlorophenyl)methylene]-, methyl ester
• CAS NO: 76862-09-4
• Molecular Formula: C10H10ClNO2
• Molecular Weight: 211.648
• Mol File: 76862-09-4.mol
• Article Data: 41

Chemical Properties

• CAS DataBase Reference: Glycine, N-[(4-chlorophenyl)methylene]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[(4-chlorophenyl)methylene]-, methyl ester(76862-09-4)
• EPA Substance Registry System: Glycine, N-[(4-chlorophenyl)methylene]-, methyl ester(76862-09-4)

Safety Data

• Hazardous Substances Data: 76862-09-4(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 616-34-2 methoxycarbonylmethylamine 
• 6000-43-7 2-aminoethanoic acid hydrochloride 
• 5680-79-5 glycine ethyl ester hydrochloride 

Downstream Products

• 113845-88-8 2-{[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-amino}-4-cyano-2-(2-cyano-ethyl)-butyric acid methyl ester 
• 67567-60-6 2-(4-chloro-phenyl)-5-methoxy-oxazole 
• 1166397-84-7 (2R,4R,5S)-5-(4-chlorophenyl)-pyrrolidine-2,4-dicarboxylicacid 4-tert-butyl ester 2-methyl ester 
• 1166397-85-8 trimethyl (2R,3R,4R,5S)-5-(4-chlorophenyl)pyrrolidine-2,3,4-tricarboxylate 
• 1100793-02-9 methyl (1S,3R,3aS,6aR)-3-(4-chlorophenyl)-octahydro-4-oxocyclopenta[c]pyrrole-1-carboxylate 
• 1221295-36-8 C₂₇H₂₄ClNO₃ 
• 1221295-28-8 methyl (2S,3R,4S,5R)-4-(4-chlorobenzoyl)-3phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate 
• 1221295-31-3 methyl (2S,3R,4S,5R)-4-benzoyl-3-(4-chlorophenyl)-5-(4-chlorophenyl)pyrrolidine-2-carboxylate 
• 1221295-30-2 C₂₉H₂₄ClNO₃ 

Relevant articles and documents

'Bis-ornithine' (2,2-bis(aminopropyl)glycine): a new tetravalent template for assembling different functional peptides

Synthesis of bis-ornithine, a new Cα,α-disubstituted α-amino acid bearing orthogonally protected α and δ amine groups is reported. Bis-ornithine (bisOrn) and dipeptides containing bis-ornithine have been synthesized in solution up to multigram

Copper/GanPhos-Catalyzed 1,3-Dipolar Cycloaddition of Azo?-methine Ylides: An Efficient Access to Chiral Pyrrolidine Spirocycles

A highly efficient copper/GanPhos-catalyzed 1,3-dipolar cyclo?-addition?-of azomethine ylides is reported. This viable transformation provides a series of optically active spiro[dihydronaphthalene-2,3′-pyrrolidine]s, bearing one spiro quaternary and three tertiary stereogenic centers, in good yields and with high ee values. This protocol features high diastereo- A nd enantioselectivity, broad substrate scope and mild reaction conditions.

Silver/palladium relay catalyzed 1,3-dipole annulation/allylation reactions to access fully substituted allyl imidazolidines

A silver/palladium relay catalyzed 1,3-dipole annulation/allylation reaction of iminoesters and Baylis-Hillman acetates for the construction of fully substituted allyl imidazolidines is reported. The reaction of both iminoesters and Baylis-Hillman acetate