Basic Description

Synonyms	Fmoc-Met-OPfp \| 86060-94-8 \| (2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylsulfanylbutanoate \| Fmoc-L-Met-OPfp \| SCHEMBL17151010 \| DTXSID80544412 \| OKDPSRDTLNXPFQ-SFHVURJKSA-N \| MFCD00065665 \| AKOS015853423 \| AKOS015902598 \| CS-W009606 \| HY
Specifications & Purity	≥96%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Methionine and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Methionine and derivatives
Alternative Parents	Alpha amino acid esters Fluorenes Phenol esters Phenoxy compounds Fatty acid esters Fluorobenzenes Aryl fluorides Carbamate esters Carboxylic acid esters Monocarboxylic acids and derivatives Dialkylthioethers Sulfenyl compounds Organic oxides Carbonyl compounds Organofluorides Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Methionine or derivatives - Alpha-amino acid ester - Fluorene - Phenol ester - Phenoxy compound - Fatty acid ester - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Carbamic acid ester - Carboxylic acid ester - Dialkylthioether - Sulfenyl compound - Thioether - Monocarboxylic acid or derivatives - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504767447
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504767447
IUPAC Name	(2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylsulfanylbutanoate
INCHI	InChI=1S/C26H20F5NO4S/c1-37-11-10-18(25(33)36-24-22(30)20(28)19(27)21(29)23(24)31)32-26(34)35-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,32,34)/t18-/m0/s1
InChIKey	OKDPSRDTLNXPFQ-SFHVURJKSA-N
Smiles	CSCCC(C(=O)OC1=C(C(=C(C(=C1F)F)F)F)F)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Isomeric SMILES	CSCC[C@@H](C(=O)OC1=C(C(=C(C(=C1F)F)F)F)F)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
WGK Germany	3
PubChem CID	13585949
Molecular Weight	537.5
Beilstein	4732241

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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7 results found

Lot Number	Certificate Type	Date	Item
E1616041	Certificate of Analysis	Jan 11, 2024	F116839
H2308582	Certificate of Analysis	Mar 17, 2023	F116839
H2308578	Certificate of Analysis	Mar 17, 2023	F116839
H2308545	Certificate of Analysis	Mar 17, 2023	F116839
H2308479	Certificate of Analysis	Mar 17, 2023	F116839
H2308575	Certificate of Analysis	Mar 17, 2023	F116839
H2308531	Certificate of Analysis	Mar 17, 2023	F116839

Chemical and Physical Properties

Molecular Weight	537.500 g/mol
XLogP3	6.100
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	10
Rotatable Bond Count	10
Exact Mass	537.103 Da
Monoisotopic Mass	537.103 Da
Topological Polar Surface Area	89.900 Å²
Heavy Atom Count	37
Formal Charge	0
Complexity	758.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Documents & Articles

Solid-Phase Peptide Synthesis (SPPS) — Efficient Strategies and Innovative Techniques

Categories: Technical articles

Tags:

Chemical synthesis Amino acids Protein Biology Acids Solvents Carbohydrates Peptides Peptide synthesis reagents Organic blocks SPPS Peptide synthesis Protection groups

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SKU	Size	Availability	Price
F116839-1g	1g	3	$32.90
F116839-5g	5g	3	$79.90
F116839-25g	25g	3	$356.90

Fmoc-Met-OPfp - 96%, high purity , CAS No.86060-94-8