20902-47-0

Basic information

• Product Name: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-, methyl ester
• CAS NO: 20902-47-0
• Molecular Formula: C20H30N2O5
• Molecular Weight: 378.469
• Mol File: 20902-47-0.mol
• Article Data: 43

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-, methyl ester(20902-47-0)
• EPA Substance Registry System: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-, methyl ester(20902-47-0)

Safety Data

• Hazardous Substances Data: 20902-47-0(Hazardous Substances Data)

Upstream product

• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 141468-55-5 4-isopropyl-2,5-dioxo-oxazolidine-3-carboxylic acid-tert-butyl ester 
• 13734-41-3 t-Boc-L-valine 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 67-56-1 methanol 
• 51987-73-6 (S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester 
• 50903-49-6 2(S)-((tert-butoxycarbonyl)amino)-3-methyl-butyric acid 2,3,4,5,6-pentafluorophenyl ester 
• 187884-05-5 (2S)-2-[(tert-butoxycarbonyl)amino]-3-methylbutanethioic S-acid 
• 63-91-2 L-phenylalanine 
• 72-18-4 L-valine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 100-39-0 benzyl bromide 
• 51803-69-1 methyl 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanamido)acetate 
• 66447-55-0 ((S)-1-benzylcarbamoyl-2-methyl-propyl)-carbamic acid tert-butyl ester 

Downstream Products

• 1447815-56-6 L-isoseryl-L-valyl-L-phenylalanine 
• 78123-60-1 methyl (S)-2-<<(tert-butoxycarbonyl)-(S)-leucinyl-(S)-valinyl>amino>-3-phenylpropanoate 
• 52828-91-8 H-Leu-Val-Phe-OMe 
• 89821-19-2 NH₂-L-Phe-L-Val-CH₃*TFA 
• 218785-67-2 (S)-2-{(S)-2-[(2-Bromo-ethyl)-(2-nitro-benzenesulfonyl)-amino]-3-methyl-butyrylamino}-3-phenyl-propionic acid methyl ester 
• 218785-73-0 (S)-2-[(S)-3-Isopropyl-4-(2-nitro-benzenesulfonyl)-2-oxo-piperazin-1-yl]-3-phenyl-propionic acid methyl ester 
• 218785-61-6 (S)-2-[(S)-3-Methyl-2-(2-nitro-benzenesulfonylamino)-butyrylamino]-3-phenyl-propionic acid methyl ester 
• 602297-80-3 2,6-dimethoxybenzoyl-Val-Phe-OMe 
• 175444-86-7 [(S)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid tert-butyl ester 
• 3918-92-1 L-valyl L-phenylalanine 

Relevant articles and documents

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Synthesis of a natural glycine-rich heptacyclopeptide - mahafacyclin A (7) was accomplished by solution-phase technique of peptide synthesis via coupling of tetrapeptide unit Boc-L-Thr-L-Ile-L-Leu-Gly-OH with tripeptide unit L-Val-L-Phe-Gly-OMe followed b

Pd-Catalyzed Site-Selective C(sp2)-H Olefination and Alkynylation of Phenylalanine Residues in Peptides

Pd-catalyzed site-selective C(sp2)-H olefination and alkynylation of phenylalanine residues in peptides are described. The amino acids within the peptides are used as native bidentate directing groups to facilitate C-H functionalization. This p

Pd-catalyzed intramolecular C(sp2)-H amination of phenylalanine moieties in dipeptides: Synthesis of indoline-2-carboxylate-containing dipeptides

A palladium-catalyzed intramolecular C(sp2)-H amination of phenylalanine moieties in dipeptides is described. By this protocol, a series of indoline-2-carboxylate-containing dipeptides were synthesized from dipeptides. The N-protected amino aci