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Fmoc-N-(3-Boc-aminopropyl)-Gly-OH

Base Information Edit
  • Chemical Name:Fmoc-N-(3-Boc-aminopropyl)-Gly-OH
  • CAS No.:143192-31-8
  • Molecular Formula:C25H30N2O6
  • Molecular Weight:454.523
  • Hs Code.:29225090
  • DSSTox Substance ID:DTXSID10373277
  • Nikkaji Number:J499.474D
  • Wikidata:Q82161431
  • Mol file:143192-31-8.mol
Fmoc-N-(3-Boc-aminopropyl)-Gly-OH

Synonyms:143192-31-8;Fmoc-N-(3-Boc-aminopropyl)-Gly-OH;Fmoc-Norn(Boc)-OH;Fmoc-N-(3-Boc-aminopropyl)-glycine;2-[9H-fluoren-9-ylmethoxycarbonyl-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]acetic acid;N-[3-(Boc-amino)propyl]-N-Fmoc-glycine;N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-(3-((tert-butoxycarbonyl)amino)propyl)glycine;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(3-((tert-butoxycarbonyl)amino)propyl)amino)acetic acid;fmoc-norn(boc)-oh, AldrichCPR;SCHEMBL16060804;DTXSID10373277;Fmoc-{Boc-NH(CH2)3}Gly-OH;MFCD04112688;AKOS015911502;CS-0320928;E70682;J-007761;[[3-[[[tert-Butyloxy]carbonyl]amino]propyl][[(9H-fluoren-9-yl)methoxy]carbonyl]amino]acetic acid;2-((((9H-fluoren-9-yl)methoxy)carbonyl)(3-(tert-butoxycarbonylamino)propyl)amino)acetic acid

Suppliers and Price of Fmoc-N-(3-Boc-aminopropyl)-Gly-OH
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
  • TRC
  • Fmoc-N-(3-Boc-aminopropyl)-glycine
  • 100mg
  • $ 90.00
  • TRC
  • Fmoc-N-(3-Boc-aminopropyl)-glycine
  • 50mg
  • $ 60.00
  • American Custom Chemicals Corporation
  • FMOC-NORN(BOC)-OH 95.00%
  • 100MG
  • $ 560.00
  • American Custom Chemicals Corporation
  • FMOC-NORN(BOC)-OH 95.00%
  • 5MG
  • $ 495.42
  • AK Scientific
  • Fmoc-Norn(Boc)-OH
  • 1g
  • $ 623.00
  • Activate Scientific
  • N-[3-(Boc-amino)propyl]-N-Fmoc-glycine 95%
  • 5 g
  • $ 1196.00
  • Activate Scientific
  • N-[3-(Boc-amino)propyl]-N-Fmoc-glycine 95%
  • 1 g
  • $ 358.00
  • Acrotein
  • N-[3-(Boc-amino)propyl]-N-Fmoc-glycine 97%
  • 0.5g
  • $ 183.33
Total 6 raw suppliers
Chemical Property of Fmoc-N-(3-Boc-aminopropyl)-Gly-OH Edit
Chemical Property:
  • Boiling Point:649.3±48.0 °C(Predicted) 
  • PKA:3.88±0.10(Predicted) 
  • PSA:105.17000 
  • Density:1.232±0.06 g/cm3(Predicted) 
  • LogP:4.62780 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:11
  • Exact Mass:454.21038668
  • Heavy Atom Count:33
  • Complexity:669
Purity/Quality:

99% *data from raw suppliers

Fmoc-N-(3-Boc-aminopropyl)-glycine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NCCCN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
Technology Process of Fmoc-N-(3-Boc-aminopropyl)-Gly-OH

There total 6 articles about Fmoc-N-(3-Boc-aminopropyl)-Gly-OH 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:
{[3-(tert-Butoxycarbonylamino)propyl]amino}acetic acid ethyl ester; With sodium hydroxide; In 1,4-dioxane; methanol; at 20 ℃; for 1h;
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide; In water; acetonitrile; at 20 ℃; for 16h;
DOI:10.3390/molecules24244429
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) Et3N, MgSO4, 2.) NaBH4 / 1.) MeOH, room temperature, 1.5 h, 2.) MeOH, -5 deg C (1.5 h), 0 deg C (1 h)
2: 100 percent / diisopropylethylamine / dimethylformamide / 1.) 0 deg C, 30 min, 2.) room temperature, 3 h
3: 74 percent / H2 / Pd/C / methanol / 4 h / 3102.9 Torr / Ambient temperature
4: 85 percent / aq. Et3N / acetonitrile / 4 h / Ambient temperature
With sodium tetrahydroborate; hydrogen; magnesium sulfate; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo961580e
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