CAS 71989-28-1
:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-methionine
Description:
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-methionine, commonly referred to as Fmoc-L-methionine, is a derivative of the amino acid methionine, modified with a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where the Fmoc group serves as a protective moiety for the amino group of the amino acid. The Fmoc group is stable under basic conditions but can be easily removed under mildly acidic conditions, allowing for selective deprotection during peptide assembly. Fmoc-L-methionine is characterized by its relatively high stability, solubility in organic solvents, and compatibility with various coupling reagents used in peptide synthesis. Additionally, methionine is an essential amino acid, playing a crucial role in protein synthesis and various metabolic processes. The presence of the fluorenyl group enhances the compound's photophysical properties, making it useful in applications involving fluorescence. Overall, Fmoc-L-methionine is a valuable building block in the field of biochemistry and pharmaceutical research.
Formula:C20H21NO4S
InChI:InChI=1S/C20H21NO4S/c1-26-11-10-18(19(22)23)21-20(24)25-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-/m0/s1
InChI key:InChIKey=BUBGAUHBELNDEW-SFHVURJKSA-N
SMILES:C(OC(N[C@@H](CCSC)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:- (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-methylsulfanylbutanoic acid
- (2S)-2-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-4-(methylsulfanyl)butanoic acid
- (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfanyl)butanoic acid
- (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-(methylsulfanyl)butanoate
- (S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-4-methylsulfanylbutanoic acid
- (S)-N-Fmoc-methionine
- 224: PN: US20070042401 PAGE: 30 claimed protein
- 915: PN: WO2006135786 PAGE: 59 claimed protein
- <span class="text-smallcaps">L</span>-Fmoc-Methionine
- <span class="text-smallcaps">L</span>-Methionine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
- FMOC-methionine
- Fmoc-L-Met-OH
- Fmoc-Met-OH
- N-(9-Fluorenylmethoxycarbonyl)-<span class="text-smallcaps">L</span>-methionine
- N-(9-Fluorenylmethoxycarbonyl)-L-methionine
- N-(9-Fluorenylmethoxycarbonyl)methionine
- N-Fluorenylmethoxycarbonyl-<span class="text-smallcaps">L</span>-methionine
- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-methionine
- N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-methionine
- N-alpha-FMOC-L-methionine
- NSC 334292
- N-Fluorenylmethoxycarbonyl-L-methionine
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 15 products.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-methionine
CAS:Formula:C20H21NO4SPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:371.45Fmoc-Met-OH
CAS:<p>M03368 - Fmoc-Met-OH</p>Formula:C20H21NO4SPurity:98%Color and Shape:Solid, Powder or Crystalline PowderMolecular weight:371.45Fmoc-Met-OH
CAS:<p>Bachem ID: 4003154.</p>Formula:C20H21NO4SPurity:99.67%Color and Shape:WhiteMolecular weight:371.46Fmoc-Met-OH
CAS:Formula:C20H21NO4SPurity:≥ 98.0%Color and Shape:White to almost white powder or colourless crystalsMolecular weight:371.46L-Methionine-d3-N-FMOC(S-methyl-d3)
CAS:Formula:CD3SCH2CH2CH(NHFMOC)COOHPurity:98 atom % DColor and Shape:White Solid.Molecular weight:374.47Fmoc-Met-OH
CAS:<p>Fmoc-Met-OH (Fmoc-L-Met-OH) is an fmoc-based programmed synthesis of methionine derivatives.</p>Formula:C20H21NO4SPurity:99.55%Color and Shape:SolidMolecular weight:371.45Fmoc-Met-OH
CAS:<p>Fmoc-Met-OH is an amino acid that has significant cytotoxicity. It is a neutral molecule with a pKa of 7.6, and is soluble in water at low pH. The hydrogen bonding interactions of Fmoc-Met-OH are strong and involve the amino group and the side chain carboxyl groups, as well as other hydrophobic interactions with aromatic rings. Fmoc-Met-OH is also an acid analysis reagent for chlorine atoms because it can be easily converted to methoxychlor (CHClO). Fmoc-Met-OH has been shown to inhibit epidermal growth factor receptor signaling and has been used to block epidermal growth factor induced cell cycle progression in cancer cells.</p>Formula:C20H21NO4SPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:371.5 g/molFMOC-L-Methionine extrapure, 99%
CAS:Formula:C20H21NO4SPurity:min. 99%Color and Shape:White, Crystalline powderMolecular weight:371.46L-Fmoc-Methionine- 34S
CAS:Controlled ProductFormula:C20H21NO4SColor and Shape:NeatMolecular weight:373.35












