51769-52-9

Upstream product

• 56-41-7 L-alanin 
• 122-04-3 4-nitro-benzoyl chloride 
• 1037-31-6 4-nitrophenyl 4-nitrobenzoate 
• 606938-44-7 tert-Butyl(2S)-2-[(4-nitrobenzoyl)amino]-propanoate 

Downstream Products

• 93709-76-3 4-NO₂Bz-L-Ala-L-PheOMe 
• 93710-02-2 4-NO₂Bz-D-Ala-L-PheOMe 
• 56-41-7 L-alanin 
• 62-23-7 4-nitro-benzoic acid 
• 93709-77-4 4-NO₂Bz-L-Ala-L-ValOMe 
• 93710-03-3 4-NO₂Bz-D-Ala-L-ValOMe 
• 93709-85-4 4-ClBz-L-Ala-L-ValOMe 
• 84742-49-4 4-NO₂Bz-L-Ala-L-AlaOMe 
• 93710-01-1 4-NO₂Bz-D-Ala-L-AlaOMe 

Relevant academic research and scientific papers

Effect of the composition of the aqueous organic solvent on the kinetics of N-acylation of α-amino acids with 4-nitrophenyl 4-nitrobenzoate

Equations relating the N-acylation rate constants of glycine, L-α-alanine, DL-threonine, and L-proline with 4-nitrophenyl 4-nitrobenzoate in water-acetonitrile, water-2-propanol, and water-2-methyl-2-propanol solvents to the composition of the medium were

(4,2-Disubstituted-thiazol-5-yl)amine compounds as PDE7 inhibitors

A compound selected from those of formula (I): wherein R1a, R1b, R2, R3, are as defined in the description,and optionally, its optical isomers, N-oxide, and addition salts thereof with a pharmaceutically-accepta

Synthesis and aldose reductase inhibitory activity of benzoyl-amino acid derivatives

A series of N-(4-methoxy, 4-fluoro, 4-trifluoromethyl and 4-nitrobenzoyl)-L-amino acids was synthesized and their inhibitory activity towards bovine lens aldose reductase (ALR2) was tested.

N-TERMINAL SUBSTITUENT AND SIDE-CHAIN INFLUENCES ON THE CHEMICAL SHIFTS OF PROTONS IN MODEL DIPEPTIDE SYSTEMS

(1)H Chemical shift values of ester methyls in model dipeptide esters have been shown to be sensitive to (a) the nature and configuration of the constituent amino acids and (b) the spatial distance between the N-terminal aryl group and the ester protons.C