93710-17-9

Basic information

• Product Name: L-Phenylalanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl]-, methyl ester
• CAS NO: 93710-17-9
• Molecular Formula: C28H28N2O5
• Molecular Weight: 472.541
• Mol File: 93710-17-9.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl]-, methyl ester(93710-17-9)
• EPA Substance Registry System: L-Phenylalanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl]-, methyl ester(93710-17-9)

Safety Data

• Hazardous Substances Data: 93710-17-9(Hazardous Substances Data)

Upstream product

• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 35661-39-3 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine 
• 103321-50-2 9H-fluoren-9-ylmethyl [(1S)-2-chloro-1-methyl-oxoethyl]carbamate 
• 1158245-85-2 (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanethioic S-acid 
• 128369-71-1 (S)-methyl-(N-allyloxycarbonyl)phenylalaninate 
• 142061-92-5 N-(9-fluorenylmethoxycarbonyl)-L-alanyl fluoride 
• 86060-86-8 (9H-fluoren-9-yl-methoxy)carbonyl-L-alanine pentafluorophenyl ester 
• 35661-38-2 Fmoc-alanine 

Downstream Products

• 218785-75-2 Fmoc-L-Ala-L-Phe-OH 
• 1361509-98-9 (S)-methyl 2-((S)-2-((S)-2-(benzyloxycarbonylamino)-4-methylpentanamido)propaneselenoamido)-3-phenylpropanoate 
• 1361509-54-7 (S)-methyl 2-((S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)propaneselenoamido)-3-phenylpropanoate 

Relevant articles and documents

Synthesis of Dipeptide, Amide, and Ester without Racemization by Oxalyl Chloride and Catalytic Triphenylphosphine Oxide

An efficient triphenylphosphine oxide-catalyzed amidation and esterification for the rapid synthesis of a series of dipeptides, amides, and esters is described. This reaction is applicable to challenging couplings of hindered carboxylic acids with weakly

Fast Amide Couplings in Water: Extraction, Column Chromatography, and Crystallization Not Required

In the micelle of PS-750-M, the presence of 3° amides from the surfactant proline linker mimics dimethylformamide, dimethylacetamide, and N-methyl-2-pyrrolidone. The resultant micellar properties enable extremely fast amide couplings mediated by 1-ethyl-3

Iodine-Mediated Oxidative Coupling of Hydroxamic Acids with Amines towards a New Peptide-Bond Formation

An efficient and straightforward approach for the coupling of Nα-protected hydroxamic acids with an amino component in the presence of iodine is delineated. The reaction is mediated by the formation of unstable but reactive acyl nitroso intermediates. The peptide hydroxamic acids were found to be useful substrates in coupling reactions.