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Encyclopedia

Fmoc-N-methyl-L-valine

Base Information Edit
  • Chemical Name:Fmoc-N-methyl-L-valine
  • CAS No.:84000-11-3
  • Molecular Formula:C21H23NO4
  • Molecular Weight:353.418
  • Hs Code.:2922509090
  • European Community (EC) Number:807-805-3
  • DSSTox Substance ID:DTXSID30359654
  • Nikkaji Number:J1.753.291J
  • Wikidata:Q72478704
  • Mol file:84000-11-3.mol
Fmoc-N-methyl-L-valine

Synonyms:Fmoc-N-Me-Val-OH;84000-11-3;Fmoc-N-methyl-L-valine;Fmoc-Nalpha-methyl-L-valine;(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-methylbutanoic acid;Fmoc-N-a-methyl-L-valine;(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methyl-butanoic acid;MFCD00153395;L-Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-;N-Fmoc-N-methyl-L-valine;N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valine;(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-3-methylbutanoic acid;Fmoc-MeVal-OH;Fmoc-N-Me-L-Val-OH;Fmoc-N-alpha-Methyl-L-valine;(S)-Fmoc-N-methylvaline;Fmoc-N-|A-Methyl-L-valine;N-Methyl-N-Fmoc-L-Val-OH;SCHEMBL118228;DTXSID30359654;N-(((9H-fluoren-9-yl)methoxy)carbonyl)-N-methyl-L-valine;HY-I1112;AKOS016843073;AKOS022171440;AKOS022186577;AKOS022186588;AC-8572;AM82391;CS-W009268;(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)amino}-3-methylbutanoic acid;AS-19173;F1165;F12344;M03379;EN300-1666771;J-300311;Fmoc-N-Me-Val-OH, >=98.0% (sum of enantiomers, HPLC);N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-alpha-methyl-L-valine

Suppliers and Price of Fmoc-N-methyl-L-valine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Fmoc-N-methyl-L-valine
  • 1g
  • $ 333.00
  • TRC
  • Fmoc-N-Me-Val-OH
  • 100mg
  • $ 45.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valine >98.0%(HPLC)(T)
  • 1g
  • $ 46.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valine >98.0%(HPLC)(T)
  • 5g
  • $ 138.00
  • Sigma-Aldrich
  • Fmoc-N-Me-Val-OH ≥98.0% (sum of enantiomers, HPLC)
  • 1g
  • $ 128.00
  • Oakwood
  • Fmoc-N-Me-Val-OH 98%
  • 100g
  • $ 330.00
  • Oakwood
  • Fmoc-N-Me-Val-OH 98%
  • 10g
  • $ 55.00
  • Oakwood
  • Fmoc-N-Me-Val-OH 98%
  • 25g
  • $ 90.00
  • Oakwood
  • Fmoc-N-Me-Val-OH 98%
  • 1g
  • $ 10.00
  • Oakwood
  • Fmoc-N-Me-Val-OH 98%
  • 5g
  • $ 30.00
Total 106 raw suppliers
Chemical Property of Fmoc-N-methyl-L-valine Edit
Chemical Property:
  • Appearance/Colour:White powder 
  • Vapor Pressure:5.83E-12mmHg at 25°C 
  • Melting Point:187-190 °C 
  • Refractive Index:1.587 
  • Boiling Point:527.6 °C at 760 mmHg 
  • PKA:3.92±0.10(Predicted) 
  • Flash Point:272.9 °C 
  • PSA:66.84000 
  • Density:1.214 g/cm3 
  • LogP:3.97650 
  • Storage Temp.:2-8°C 
  • Water Solubility.:Slightly soluble in water and dimethyl formamide. 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:353.16270821
  • Heavy Atom Count:26
  • Complexity:498
Purity/Quality:

98% *data from raw suppliers

Fmoc-N-methyl-L-valine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C(C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Isomeric SMILES:CC(C)[C@@H](C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Uses N-Fmoc-N-methyl-L-valine is used as enzyme substrates and reagents, culture media additives, dyes, stains and indicators. It is also involved in the preparation of N-methylated peptides.
Technology Process of Fmoc-N-methyl-L-valine

There total 8 articles about Fmoc-N-methyl-L-valine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With triethylsilane; trifluoroacetic acid; In chloroform; for 22h; Ambient temperature;
DOI:10.1021/jo00149a016
Guidance literature:
With trifluoroacetic acid; In dichloromethane; toluene; at 20 ℃; for 1h;
DOI:10.1007/s00726-008-0221-8
Guidance literature:
With triethylsilane; aluminium trichloride; In chloroform; at 20 ℃;
DOI:10.1021/jo050916u
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