136554-94-4 Usage
Uses
Used in Pharmaceutical Industry:
FMOC-D-TRP-OPFP is used as a protecting agent for the amine group of amino acids during peptide synthesis. Its ability to protect specific functional groups allows for the controlled and efficient production of peptides with desired properties and biological activities.
Used in Chemical Research:
FMOC-D-TRP-OPFP is used as a key component in the development of novel peptide-based drugs and therapeutic agents. Its role in protecting specific amino acid functional groups enables researchers to explore new peptide sequences and structures with potential applications in various therapeutic areas.
Used in Biochemistry and Molecular Biology:
FMOC-D-TRP-OPFP is used as a reagent in the synthesis of peptides for studying protein-protein interactions, enzyme substrate specificity, and other biological processes. Its ability to protect specific functional groups allows for the controlled synthesis of peptides with defined structures, facilitating the investigation of their biological functions and mechanisms of action.
Overall, FMOC-D-TRP-OPFP plays a vital role in the production of peptides and the development of new therapeutic agents, making it an essential component in various applications across the pharmaceutical, chemical research, and biochemistry industries.
Check Digit Verification of cas no
The CAS Registry Mumber 136554-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,5 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136554-94:
(8*1)+(7*3)+(6*6)+(5*5)+(4*5)+(3*4)+(2*9)+(1*4)=144
144 % 10 = 4
So 136554-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C32H21F5N2O4/c33-25-26(34)28(36)30(29(37)27(25)35)43-31(40)24(13-16-14-38-23-12-6-5-7-17(16)23)39-32(41)42-15-22-20-10-3-1-8-18(20)19-9-2-4-11-21(19)22/h1-12,14,22,24,38H,13,15H2,(H,39,41)/t24-/m1/s1
136554-94-4Relevant articles and documents
PREPARATION OF PENTAFLUOROPHENYL ESTERS OF FMOC PROTECTED AMINO ACIDS WITH PENTAFLUOROPHENYL TRIFLUOROACETATE
Green, Michael,Berman, Judd
, p. 5851 - 5852 (1990)
A high yield procedure for the preparation of pentafluorophenyl esters of Nα-9-fluorenylmethyloxycarbonyl protected amino acids is described.The procedure utilizes pentafluorophenyl trifluoroacetate.
9-Fluorenylmethyl Pentafluorophenyl Carbonate as a Useful Reagent for the Preparation of N-9-Fluorenylmethyloxycarbonylamino Acids and their Pentafluorophenyl Esters
Schoen, Istvan,Kisfaludy, Lajos
, p. 303 - 305 (2007/10/02)
9-Fluorenylmethyl pentafluorophenyl carbonate is a useful reagent for the efficient, side reaction-free introduction of N-9-fluorenylmethyloxycarbonyl protecting group into amino acids and for the subsequent preparation of their pentafluorophenyl esters.Some new compounds of both types are described.
