Fmoc-met(O2)-OH

Base Information

• Chemical Name: Fmoc-met(O2)-OH
• CAS No.: 163437-14-7
• Molecular Formula: C20H21NO6S
• Molecular Weight: 403.45
• Hs Code.: 2930 90 98
• European Community (EC) Number: 830-708-2
• DSSTox Substance ID: DTXSID80426825
• Wikidata: Q72478512
• Mol file: 163437-14-7.mol

Synonyms:FMOC-MET(O2)-OH;163437-14-7;Fmoc-L-methionine sulfone;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylsulfonylbutanoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylsulfonyl)butanoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)-amino)-4-(methylsulfonyl)butanoic acid;Fmoc-L-Met(O2)-OH;fmoc-met(o2)-oh, AldrichCPR;SCHEMBL3378520;DTXSID80426825;MFCD00153361;AKOS015911878;AM82148;DS-4813;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(methylsulfonyl)butanoic acid;CS-0101105;EN300-636707;F10673;M06257;(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methanesulfonylbutanoic acid;Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfonyl)-, (2S)-;N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-methioninesulfon (Fmoc-L-Met(O2)-OH)

Chemical Property of Fmoc-met(O2)-OH

Chemical Property:

• Boiling Point: 709.476 °C at 760 mmHg
• PKA: 3.52±0.10(Predicted)
• Flash Point: 382.877 °C
• PSA: 118.15000
• Density: 1.359 g/cm³
• LogP: 3.88470
• Storage Temp.: Store at RT.
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 403.10895856
• Heavy Atom Count: 28
• Complexity: 651

Purity/Quality:

98%,99%, ^*data from raw suppliers

Fmoc-L-methionine sulfone ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CS(=O)(=O)CCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
• Isomeric SMILES: CS(=O)(=O)CC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
• Description: FMOC-Met (O2)-OH is the N-alpha protected form of L-methionine mediated by FMOC group (9-Fluorenylmethyloxycarbonyl). It is useful to act as a building block in peptide synthesis. For example, it, as well as its derivative Tbfmoc-Met-OH can be used as a building block for the solid phase synthesis of ubiquitin C-hydrazide. It can also be used for synthesizing some novel cyclic peptides with pharmacological effects such as treatment of inflammatory disease.