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

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

Uses

Used in Pharmaceutical Industry:
Fmoc-D-Cys(Trt)-OPfp is used as a building block for the synthesis of bioactive peptides and proteins. Its application is crucial for the development of new drugs and therapeutic agents, as it enables the controlled and selective assembly of peptide chains, leading to the production of specific and effective bioactive molecules.
Used in Research and Development:
In the field of research and development, Fmoc-Cys(Trt)-OPfp serves as a valuable tool for studying the structure and function of peptides and proteins. Its use in peptide synthesis allows researchers to create and modify peptide sequences, enabling the investigation of their biological activities and potential applications in various therapeutic areas.
Used in Peptide Synthesis:
Fmoc-D-Cys(Trt)-OPfp is used as a key component in the solid-phase peptide synthesis (SPPS) technique. Its presence allows for the stepwise and controlled addition of amino acids to a growing peptide chain, ensuring the correct sequence and minimizing side reactions. This method is widely employed in the production of peptides for various applications, including drug development, diagnostics, and research.
Used in Biochemistry and Molecular Biology:
Fmoc-D-Cys(Trt)-OPfp is utilized in the study of protein structure and function, as well as in the development of novel bioconjugation techniques. Its ability to form stable peptide bonds makes it an essential component in the synthesis of chimeric molecules, protein-drug conjugates, and other bioactive compounds with potential applications in medicine and biotechnology.

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