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FMOC-D-MET-OPFP is a chemical compound that combines FMOC-D-MET, an amino acid derivative featuring a fluorenylmethyloxycarbonyl (FMOC) protecting group, with OPFP, a phosphonium ester. The FMOC group is widely utilized in peptide synthesis to shield the amino group of the amino acid, ensuring controlled reactions. OPFP serves as a selective reagent for the labeling and modification of proteins and peptides. FMOC-D-MET-OPFP is designed for the precise and controlled alteration of target proteins and peptides, proving to be an indispensable tool in the realms of protein and peptide chemistry.
Used in Chemical Biology and Biochemical Research:
FMOC-D-MET-OPFP is used as a reagent for the modification and labeling of peptides and proteins. Its unique structure facilitates selective and controlled chemical modifications, which is crucial for studying protein functions and interactions within biological systems.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-D-MET-OPFP is used as a protected amino acid derivative. The FMOC protecting group on the amino group prevents unwanted side reactions during the synthesis process, allowing for the stepwise assembly of peptide chains with high precision.
Used in Protein Engineering:
FMOC-D-MET-OPFP is utilized as a component in protein engineering, where it aids in the construction of novel proteins with specific functions. FMOC-D-MET-OPFP's ability to selectively modify peptides and proteins enables the creation of proteins with tailored properties for various applications.
Used in Drug Development:
In the pharmaceutical industry, FMOC-D-MET-OPFP is employed in the development of new drugs. Its role in the selective modification of peptides and proteins can lead to the discovery of bioactive molecules with potential therapeutic applications.
Used in Diagnostics:
FMOC-D-MET-OPFP is also used in the development of diagnostic tools. FMOC-D-MET-OPFP's capacity for selective protein and peptide labeling can contribute to the creation of sensitive and specific diagnostic assays for detecting diseases or monitoring treatment efficacy.

210473-10-2

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210473-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210473-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,4,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 210473-10:
(8*2)+(7*1)+(6*0)+(5*4)+(4*7)+(3*3)+(2*1)+(1*0)=82
82 % 10 = 2
So 210473-10-2 is a valid CAS Registry Number.

210473-10-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) (2R)-2-(9H-fluoren-9-ylmethoxycarbo nylamino)-4-methylsulfanyl-butanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:210473-10-2 SDS

210473-10-2Relevant academic research and scientific papers

Synthesis of aryl esters of protected amino acids from aryl sulfonates

Pudhom, Khanitha,Vilaivan, Tirayut

, p. 5939 - 5942 (2007/10/03)

Aryl esters of Boc- and Fmoc-protected amino acids derived from electron-deficient phenols have been prepared in good yields from aryl 4- nitrobenzenesulfonates in the presence of 1-hydroxy-benzotriazole as catalyst.

A new facile one-pot preparation of pentafluorophenyl (Pfp) and 3,4-dihydro-4-oxo-1,2,3-benzotriazine-3-yl (Dhbt) esters of Fmoc amino acids

Jacobsen, Mogens Havsteen,Buchardt, Ole,Engdahl, Tom,Holm, Arne

, p. 6199 - 6202 (2007/10/02)

A new one-pot procedure for the preparation of pentafluorophenyl and 3,4-dihydro-4-oxo-1,2,3-benzotriazine-3-yl esters of Nα-9-fluorenylmethyloxycarbonyl amino acids bearing no side chain protecting groups is described. The method gives the desired activated esters in high yield and purity without use of the highly allergenic DCC.

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.

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