87297-14-1

Basic information

• Product Name: L-Proline, 1-L-phenylalanyl-, phenylmethyl ester, monohydrochloride
• CAS NO: 87297-14-1
• Molecular Formula: C21H24N2O3.ClH
• Molecular Weight: 388.894
• Mol File: 87297-14-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: L-Proline, 1-L-phenylalanyl-, phenylmethyl ester, monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: L-Proline, 1-L-phenylalanyl-, phenylmethyl ester, monohydrochloride(87297-14-1)
• EPA Substance Registry System: L-Proline, 1-L-phenylalanyl-, phenylmethyl ester, monohydrochloride(87297-14-1)

Safety Data

• Hazardous Substances Data: 87297-14-1(Hazardous Substances Data)

Upstream product

• 16652-71-4 benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride 
• 124980-30-9 N-carbobenzoxy-L-proline phenylmethyl ester 
• 41324-66-7 H-Pro-OBzl 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 119153-87-6 (C₅H₉O₂)C₉H₉NO(O)(CO₂C₂H₅) 
• 70462-58-7 benzyl (tert-butoxycarbonyl)-L-phenylalanyl-L-prolinate 

Downstream Products

• 109539-08-4 BocThrPheProOBzl 
• 137372-39-5 Boc-Gly-Phe-Pro-OBzl 
• 1270202-28-2 Boc-GFGFP-OH 
• 1270202-38-4 C₄₄H₅₂FN₇O₈ 
• 1270202-56-6 C₂HF₃O₂*C₃₉H₄₄FN₇O₆ 
• 1374975-58-2 C₄₃H₅₄N₆O₉ 
• 1173882-19-3 (6S,9S,12S,14aS,20S,23S,25aS)-20-benzyl-6,12-di((S)-sec-butyl)-9-(hydroxymethyl)-23-isobutylhexadecahydro-1H-dipyrrolo[1,2-a:1',2'-j][1,4,7,10,13,16,19]heptaazacyclohenicosine-5,8,11,14,19,22,25(25aH)heptaone 
• 1270202-61-3 Boc-GE(OcHx)GFP-OH 
• 96625-35-3 ((2R,5S,10aS,10bS)-5-Benzyl-10b-hydroxy-3,6-dioxo-octahydro-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-carbamic acid tert-butyl ester 
• 96648-50-9 ((2S,5S,10aS,10bS)-5-Benzyl-10b-hydroxy-3,6-dioxo-octahydro-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-carbamic acid tert-butyl ester 
• 96625-30-8 Boc-Gly(OH)-Phe-Pro-ONp 
• 96625-29-5 Boc-Gly(OH)-Phe-Pro-OH 
• 109539-09-5 HThrPheProOBzl 
• 98908-44-2 N-benzyloxycarbonyl-L-tyrosyl-L-valyl-L-prolyl-L-leucyl-L-phenylalanyl-L-proline benzyl ester 

Relevant articles and documents

An improved route for the synthesis of Rolloamide B

A high yielding method for the synthesis of the cyclic heptapeptide Rolloamide B has been described. An effective isobutyl chloroformate (IBCF) mediated direct coupling reaction was introduced to improve the synthetic route towards Rolloamide B. Furthermo

Synthesis of elastin based peptides conjugated to benzisoxazole as a new class of potent antimicrobials - A novel approach to enhance biocompatibility

The peptides of elastin sequences chosen for the present study included tetrapeptides, pentapeptides and tricosapeptides (30 amino acids), synthesized by classical solution phase method and conjugated to [3-(4-piperidyl)-6-fluoro- 1,2-benzisoxazole]. The

Non-linear hydrophobic-induced pKa shifts: Implications for efficiency of conversion to chemical energy

By using one Asp or one Glu per thirty residues in a polytricosapeptide capable of exhibiting a hydrophobic folding and assembly transition and stepwise converting a set of the five Val residues( most proximal to the Asp or Glu residue) to more-hydrophobi