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Boc-Asp-OtBu

Base Information Edit
  • Chemical Name:Boc-Asp-OtBu
  • CAS No.:34582-32-6
  • Molecular Formula:C13H23NO6
  • Molecular Weight:289.329
  • Hs Code.:2924 19 00
  • European Community (EC) Number:840-509-2
  • DSSTox Substance ID:DTXSID40426664
  • Nikkaji Number:J304.059C
  • Wikidata:Q72448563
  • Mol file:34582-32-6.mol
Boc-Asp-OtBu

Synonyms:Boc-Asp-OtBu;34582-32-6;(S)-4-(tert-butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid;N-tert-Boc-L-aspartic Acid tert-Butyl Ester;(3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid;Boc-L-Aspartic acid 1-tert-butyl ester;(3S)-4-(tert-butoxy)-3-{[(tert-butoxy)carbonyl]amino}-4-oxobutanoic acid;N-Boc-L-aspartic Acid 1-(tert-Butyl) Ester;MFCD00038272;Boc-L-Asp-OtBu;Boc-Asp-O-t-Butyl;SCHEMBL1235160;a-tert-Butyl-N-Boc-L-aspartate;1-tert-Butyl N-Boc-L-aspartate;DTXSID40426664;RAUQRYTYJIYLTF-QMMMGPOBSA-N;AKOS015892678;AC-8610;CS-W007573;DS-1659;HY-W007573;Boc-Asp-OtBu, >=97.0% (TLC);PD196485;N-Boc-L-aspartic Acid 1-tert-Butyl Ester;AM20090540;B4618;EN300-205979;1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate;N-tert-butyloxycarbonyl-O-tert-butyl-L-aspartic acid;Q-102762;F0001-1005;N-tert-Butoxycarbonyl-L-aspartic acid 1-tert-butyl ester;N-(tert-Butoxycarbonyl)-L-aspartic Acid 1-tert-Butyl Ester;(s)-4-t-butoxy-3-(t-butoxycarbonylamino)-4-oxobutanoic acid;N-alpha-t-Butyloxycarbonyl-L-aspartic acid-alpha-t-butylester;(S)-4-tert-butoxy-3-(tert-butoxycarbonylamino)-4-oxobutanoic acid;(3S)-4-tert-butoxy-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid

Suppliers and Price of Boc-Asp-OtBu
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
  • N-tert-Boc-L-aspartic Acid tert-Butyl Ester
  • 1g
  • $ 403.00
  • Usbiological
  • N-tert-Boc-L-aspartic acid tert-butyl ester
  • 5g
  • $ 319.00
  • TRC
  • N-tert-Boc-L-asparticAcidtert-ButylEster
  • 25g
  • $ 60.00
  • TRC
  • N-tert-Boc-L-asparticAcidtert-ButylEster
  • 5g
  • $ 50.00
  • TCI Chemical
  • 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate >95.0%(HPLC)(T)
  • 1g
  • $ 38.00
  • TCI Chemical
  • 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate >95.0%(HPLC)(T)
  • 5g
  • $ 94.00
  • Sigma-Aldrich
  • Boc-Asp-OtBu Novabiochem?
  • 25 g
  • $ 962.00
  • Sigma-Aldrich
  • Boc-Asp-OtBu Novabiochem . CAS 34582-32-6, molar mass 289.33 g/mol., Novabiochem
  • 8530320025
  • $ 929.00
  • Sigma-Aldrich
  • Boc-Asp-OtBu ≥97.0% (TLC)
  • 5g
  • $ 753.00
  • Sigma-Aldrich
  • Boc-Asp-OtBu Novabiochem . CAS 34582-32-6, molar mass 289.33 g/mol., Novabiochem
  • 8530320005
  • $ 234.00
Total 105 raw suppliers
Chemical Property of Boc-Asp-OtBu Edit
Chemical Property:
  • Vapor Pressure:1.46E-08mmHg at 25°C 
  • Melting Point:101-103?C 
  • Refractive Index:1.47 
  • Boiling Point:429.011 °C at 760 mmHg 
  • PKA:4.13±0.19(Predicted) 
  • Flash Point:213.259 °C 
  • PSA:101.93000 
  • Density:1.139 g/cm3 
  • LogP:2.08700 
  • Storage Temp.:-15°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:8
  • Exact Mass:289.15253745
  • Heavy Atom Count:20
  • Complexity:377
Purity/Quality:

99% *data from raw suppliers

N-tert-Boc-L-aspartic Acid tert-Butyl Ester *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)C(CC(=O)O)NC(=O)OC(C)(C)C
  • Isomeric SMILES:CC(C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)OC(C)(C)C
  • Uses An aspartic acid derivative, Boc-Asp-OtBu can be used in stereoselective synthesis
Technology Process of Boc-Asp-OtBu

There total 13 articles about Boc-Asp-OtBu 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 hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1039/a806741d
Guidance literature:
With sodium hydroxide; In water; acetone; at 20 ℃; for 4.5h;
DOI:10.3987/COM-18-14002
Guidance literature:
With methanol; sodium hydroxide; at 20 ℃; for 3h;
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