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Fmoc-L-beta-homoalanine

Base Information
  • Chemical Name:Fmoc-L-beta-homoalanine
  • CAS No.:193954-26-6
  • Molecular Formula:C19H19NO4
  • Molecular Weight:325.364
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70941092
  • Nikkaji Number:J868.550I
  • Wikidata:Q72478449
  • Mol file:193954-26-6.mol
Fmoc-L-beta-homoalanine

Synonyms:Fmoc-L-beta-homoalanine;193954-26-6;Fmoc-|A-HoAla-OH;(3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid;(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid;fmoc-beta-homoalanine;(3S)-3-[[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO]-BUTANOIC ACID;Fmoc-|A-homoalanine;(S)-3-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic acid;MFCD00270346;(3S)-3-({[(9H-FLUOREN-9-YL)METHOXY]CARBONYL}AMINO)BUTANOIC ACID;Fmoc Protected (S)-B-Aminobutyric Acid;Fmoc-L--homoalanine;Fmoc-alfa-HoAla-OH;Fmoc-L-beta-HAla-OH;Fmoc-Ala-(C#CH2)OH;SCHEMBL119717;DTXSID70941092;LYMLSPRRJWJJQD-LBPRGKRZSA-N;AKOS015837096;CS-W009868;AC-25567;AS-31812;Fmoc-beta-Homoala-OH, >=98.0% (HPLC);EN300-816414;A813684;(S)-3-(9H-Fluoren-9-ylmethoxycarbonylamino)-butyric acid;(S)-3-(9H-Fluorene-9-ylmethoxycarbonylamino)butyric acid;3-({[(9H-Fluoren-9-yl)methoxy](hydroxy)methylidene}amino)butanoic acid

Suppliers and Price of Fmoc-L-beta-homoalanine
Supply Marketing:
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-L-beta-homoalanine
  • 250mg
  • $ 358.00
  • Usbiological
  • Fmoc-l-beta-homoalanine
  • 25mg
  • $ 312.00
  • TRC
  • Fmoc-l-β-homoalanine
  • 50mg
  • $ 75.00
  • Sigma-Aldrich
  • Fmoc-β-Homoala-OH ≥98.0% (HPLC)
  • 1g
  • $ 401.00
  • Matrix Scientific
  • Fmoc-L-beta-homoalanine
  • 1g
  • $ 446.00
  • Matrix Scientific
  • Fmoc-L-beta-homoalanine
  • 5g
  • $ 1627.00
  • Iris Biotech GmbH
  • Fmoc-L-beta-HAla-OH
  • 5 g
  • $ 1917.00
  • Crysdot
  • Fmoc-β-HoAla-OH 95+%
  • 10g
  • $ 1030.00
  • Crysdot
  • Fmoc-β-HoAla-OH 95+%
  • 25g
  • $ 1858.00
  • Crysdot
  • Fmoc-β-HoAla-OH 95+%
  • 5g
  • $ 582.00
Total 51 raw suppliers
Chemical Property of Fmoc-L-beta-homoalanine
Chemical Property:
  • Vapor Pressure:3.64E-13mmHg at 25°C 
  • Melting Point:96-98 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6)) 
  • Refractive Index:1.598 
  • Boiling Point:555.3 °C at 760 mmHg 
  • PKA:4.38±0.10(Predicted) 
  • Flash Point:289.6 °C 
  • PSA:75.63000 
  • Density:1.255 g/cm3 
  • LogP:3.77920 
  • Storage Temp.:2-8°C 
  • XLogP3:3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:325.13140809
  • Heavy Atom Count:24
  • Complexity:444
Purity/Quality:

98% *data from raw suppliers

Fmoc-L-beta-homoalanine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Isomeric SMILES:C[C@@H](CC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Uses Fmoc-l-beta-homoalanine
Technology Process of Fmoc-L-beta-homoalanine

There total 6 articles about Fmoc-L-beta-homoalanine 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 silver(I) acetate; triethylamine; In tetrahydrofuran; water;
DOI:10.1002/hlca.19980810107
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) i-BuOCOCl, NMM / 1.) THF, -20 deg C, 20 min, 2.) THF, Et2O, -5 deg C, 4 h
2: 72 percent / CF3COOAg, Et3N / tetrahydrofuran; H2O
With 4-methyl-morpholine; silver trifluoroacetate; triethylamine; isobutyl chloroformate; In tetrahydrofuran; water;
DOI:10.1002/hlca.19980810202
Guidance literature:
Multi-step reaction with 2 steps
1: tetrahydrofuran; diethyl ether / 0 °C
2: 92 percent / AgOAc, Et3N / tetrahydrofuran; H2O
With silver(I) acetate; triethylamine; In tetrahydrofuran; diethyl ether; water;
DOI:10.1002/hlca.19980810107
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