200395-72-8

Basic information

• Product Name: Fmoc-D-Cys(Trt)- OPfp
• Synonyms: (S)-perfluorophenyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(tritylthio)propanoate;N^a-FMoc-S-trityl-D-cysteine pentafluorophenyl ester, 98%;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-(triphenylmethyl)-D-cysteine pentafluorophenyl ester;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-Cys(Trt)-OPfp
• CAS NO: 200395-72-8
• Molecular Formula: C43H30F5NO4S
• Molecular Weight: 751.769
• Mol File: 200395-72-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 803.513 °C at 760 mmHg
• Flash Point: 439.749 °C
• Appearance: /
• Density: 1.36 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.62
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: Fmoc-D-Cys(Trt)- OPfp(CAS DataBase Reference)
• NIST Chemistry Reference: Fmoc-D-Cys(Trt)- OPfp(200395-72-8)
• EPA Substance Registry System: Fmoc-D-Cys(Trt)- OPfp(200395-72-8)

Safety Data

• Hazardous Substances Data: 200395-72-8(Hazardous Substances Data)

Usage

General Description

Fmoc-D-Cys(Trt)-OPfp is a chemical compound commonly used in peptide synthesis. It consists of a modified form of the amino acid cysteine, with an Fmoc (9-fluorenylmethoxycarbonyl) protecting group at the N-terminus, and a Trt (trityl) protecting group at the side chain of the cysteine residue. Additionally, it contains the OPfp (pentafluorophenyl) ester functional group, which is often used for activating carboxylic acids for amide bond formation in peptide synthesis. Fmoc-D-Cys(Trt)-OPfp enables the selective and controlled assembly of peptide chains for the efficient production of bioactive peptides and proteins.

InChI:InChI=1/C43H30F5NO4S/c44-35-36(45)38(47)40(39(48)37(35)46)53-41(50)34(49-42(51)52-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-54-43(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,49,51)/t34-/m1/s1