109074-94-4

Basic information

• Product Name: FMOC-PRO-OSU
• Synonyms: NALPHA-9-Fluorenylmethoxycarbonyl-L-proline N-hydroxysuccinimide ester;Fmoc-L-Pro-OSu;N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-proline succinimidyl ester;FMOC-L-PROLINE HYDROXYSUCCINIMIDESTER;(S)-2-[[(2,5-Dioxo-1-pyrrolidinyl)oxy]carbonyl]-1-pyrrolidinecarboxylic acid 9H-fluoren-9-ylmethyl ester;Fmoc-L-prolineN-hydroxysuccinimide ester≥ 99% (HPLC);N-Fmoc-L-proline N-succinimidyl ester;FMOC-L-PROLINE HYDROXYSUCCINIMIDE ESTER
• CAS NO: 109074-94-4
• Molecular Formula: C₂₄H₂₂N₂O₆
• Molecular Weight: 434.44
• Product Categories: Amino Acid Derivatives;Amino Acids
• Mol File: 109074-94-4.mol

Chemical Properties

• Boiling Point: 604.8±65.0 °C(Predicted)
• Appearance: /Solid
• Density: 1.43±0.1 g/cm3(Predicted)
• Refractive Index: 1.668
• Storage Temp.: Store at 0°C
• PKA: -4.05±0.40(Predicted)
• CAS DataBase Reference: FMOC-PRO-OSU(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-PRO-OSU(109074-94-4)
• EPA Substance Registry System: FMOC-PRO-OSU(109074-94-4)

Safety Data

• Hazardous Substances Data: 109074-94-4(Hazardous Substances Data)

Usage

Chemical Properties

White to off-white powder

InChI:InChI=1/C24H22N2O6/c27-21-11-12-22(28)26(21)32-23(29)20-10-5-13-25(20)24(30)31-14-19-17-8-3-1-6-15(17)16-7-2-4-9-18(16)19/h1-4,6-9,19-20H,5,10-14H2

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 71989-31-6 Fmoc-Pro-OH 

Downstream Products

• 267001-24-1 Fmoc-Pro-Ser(O-t-Bu)-Tyr(O-t-Bu)-OAll 
• 1027509-28-9 Lys(ε-Boc)-Pro-Ser(O-t-Bu)-Tyr(O-t-Bu)-OAll 
• 267001-26-3 Fmoc-Lys(ε-Boc)-Pro-Ser(O-t-Bu)-Tyr(O-t-Bu)-OAll 
• 267001-14-9 Fmoc-Ala-Lys(ε-Boc)-Pro-Ser(O-t-Bu)-Tyr(O-t-Bu)-OH 
• 267001-28-5 Fmoc-Ala-Lys(ε-Boc)-Pro-Ser(O-t-Bu)-Tyr(O-t-Bu)-OAll 
• 135904-46-0 2-{N-Benzyl-N'-[(S)-1-(2,2-dimethyl-propionyl)-pyrrolidine-2-carbonyl]-hydrazino}-N-isopropyl-acetamide 
• 136121-21-6 (S)-2-(N'-Benzyloxycarbonyl-N'-ethoxycarbonylmethyl-hydrazinocarbonyl)-pyrrolidine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester 

Relevant articles and documents

ELASTASE-SUBSTRATE, PEPTIDE LINKER IMMUNOCONJUGATES, AND USES THEREOF

The invention provides immunoconjugates of Formula I comprising a cell-binding agent linked by conjugation to one or more immunostimulatory moieties where the linker is a substrate for elastase. The invention also provides immunostimulant intermediate compositions comprising a reactive functional group. Such intermediate compositions are suitable substrates for formation of the immunoconjugates through a linker or linking moiety. The invention further provides methods of treating cancer with the immunoconjugates.

Site-Specific Incorporation of Multiple Thioamide Substitutions into a Peptide Backbone via Solid Phase Peptide Synthesis

Among various peptide modification strategies, thioamide substitution by replacing the carbonyl oxygen atom of an amide bond with a sulfur atom constitutes an invaluable tool for chemical biology, for use in peptide drug discovery and protein structure-fu

Synthesis of the repeating decapeptide unit of Mefp1 in orthogonally protected form

Mefp1 is a protein produced by the marine mussel, Mytilus edulis, which helps the organism to adhere to surfaces in turbulent waters. To better understand the nature of the adhesion process, we sought to synthesize homogeneous oligopeptides based on the repeating decapeptide unit of the protein. The fully protected decapeptide 10 has been synthesized from appropriately protected amino acid building blocks using a fragment condensation strategy. A key feature of the strategy is the late incorporation of the synthetically valuable dihydroxyproline residue. This synthesis of the orthogonally protected repeating decapeptide unit of Mefp1 represents an important first step toward producing useful quantities of homogeneous oligopeptides related to the protein.