33300-72-0

Basic information

• Product Name: BOC-ALA-PRO-OH
• Synonyms: BOC-ALA-PRO-OH;1-[N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl]-L-proline;Boc-L-Ala-L-Pro-OH;Boc-L-Ala-L-Pro;(S)-1-((S)-2-((tert-Butoxycarbonyl)amino)propanoyl)pyrrolidine-2-carboxylic acid;Boc-Ala-Pro-OH≥ 99% (TLC);Boc-Ala-Pro;Boc-AP
• CAS NO: 33300-72-0
• Molecular Formula: C₁₃H₂₂N₂O₅
• Molecular Weight: 286.32
• Mol File: 33300-72-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 491.451°C at 760 mmHg
• Flash Point: 251.021°C
• Appearance: /
• Density: 1.218g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.511
• Storage Temp.: -15°C
• CAS DataBase Reference: BOC-ALA-PRO-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-ALA-PRO-OH(33300-72-0)
• EPA Substance Registry System: BOC-ALA-PRO-OH(33300-72-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 33300-72-0(Hazardous Substances Data)

Usage

Chemical Properties

White powder

InChI:InChI=1/C13H22N2O5/c1-8(14-12(19)20-13(2,3)4)10(16)15-7-5-6-9(15)11(17)18/h8-9H,5-7H2,1-4H3,(H,14,19)(H,17,18)

Upstream product

• 330970-69-9 (S)-1-((S)-2-tert-Butoxycarbonylamino-propionyl)-pyrrolidine-2-carboxylic acid 4-phenylacetoxy-benzyl ester 

Downstream Products

• 109953-03-9 N-t-butoxycarbonyl-L-alanyl-L-prolyl-α-aza-alanine benzyl ester 
• 109953-27-7 N-t-butoxycarbonyl-L-alanyl-L-prolyl-α-azavaline benzyl ester 
• 109953-28-8 N-t-butoxycarbonyl-L-alanyl-L-prolyl-α-azanorvaline benzyl ester 
• 102721-58-4 ((S)-1-Methyl-2-{(S)-2-[(R)-2-methyl-1-(4-nitro-phenylcarbamoyl)-propylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester 
• 120792-17-8 C₉₇H₁₆₃N₁₃O₃₁ 
• 13485-59-1 L-alanyl-L-proline 
• 189573-57-7 (S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester 
• 189573-56-6 (S)-2-[((S)-1-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester 
• 189573-58-8 (S)-2-[((S)-1-{(S)-2-[(S)-2-((S)-2-{[(S)-1-((S)-2-tert-Butoxycarbonylamino-propionyl)-pyrrolidine-2-carbonyl]-amino}-propionylamino)-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester 
• 102779-11-3 [(S)-3-Methyl-1-((S)-1-methyl-2-{(S)-2-[(R)-2-methyl-1-(4-nitro-phenylcarbamoyl)-propylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-ethylcarbamoyl)-butyl]-carbamic acid tert-butyl ester 
• 102721-64-2 (S)-1-((S)-2-Amino-propionyl)-pyrrolidine-2-carboxylic acid [(R)-2-methyl-1-(4-nitro-phenylcarbamoyl)-propyl]-amide 
• 102779-12-4 (S)-1-[(S)-2-((S)-2-Amino-4-methyl-pentanoylamino)-propionyl]-pyrrolidine-2-carboxylic acid [(R)-2-methyl-1-(4-nitro-phenylcarbamoyl)-propyl]-amide 

Relevant articles and documents

Synthesis and membrane-binding properties of a characteristic lipopeptide from the membrane-anchoring domain of influenza virus A hemagglutinin

On the trail of the influenza virus! Fluorescent-labeled lipopeptides, such as the characteristic S-palmitoylated partial structure from influenza virus hemagglutinin A (see picture), can be synthesized efficiently by employing a new enzymatic protecting-group technique in the key steps. Their binding to model membranes was determined in a kinetic assay, so leading to a first approximation of the membrane-anchoring ability of the corresponding lipopeptide motif in the parent protein.