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FMOC-LYS(BOC)(ISOPROPYL)-OH

Base Information Edit
  • Chemical Name:FMOC-LYS(BOC)(ISOPROPYL)-OH
  • CAS No.:201003-48-7
  • Molecular Formula:C29H38N2O6
  • Molecular Weight:510.631
  • Hs Code.:
  • Mol file:201003-48-7.mol
FMOC-LYS(BOC)(ISOPROPYL)-OH

Synonyms:Fmoc-Lys(Boc)(isopropyl)-OH; N-(9-Fluorenylmethyloxycarbonyl)-N'-tert-butoxycarbonyl-N'-isopropyl-L-lysine

Suppliers and Price of FMOC-LYS(BOC)(ISOPROPYL)-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-l-lys(boc,ipr)-oh
  • 25mg
  • $ 90.00
  • Iris Biotech GmbH
  • Fmoc-L-Lys(Boc,iPr)-OH
  • 1 g
  • $ 337.50
  • Iris Biotech GmbH
  • Fmoc-L-Lys(Boc,iPr)-OH
  • 5 g
  • $ 1012.50
  • Crysdot
  • N-Fmoc-N'-Boc-N'-isopropyl-L-lysine 95+%
  • 25g
  • $ 772.00
  • Crysdot
  • N-Fmoc-N'-Boc-N'-isopropyl-L-lysine 95+%
  • 5g
  • $ 257.00
  • Crysdot
  • N-Fmoc-N'-Boc-N'-isopropyl-L-lysine 95+%
  • 10g
  • $ 416.00
  • ChemScene
  • Fmoc-Lys(ipr,Boc)-OH 99.30%
  • 10g
  • $ 170.00
  • ChemScene
  • Fmoc-Lys(ipr,Boc)-OH 99.30%
  • 5g
  • $ 105.00
  • ChemPep
  • Fmoc-Lys(ipr,Boc)-OH
  • 25g
  • $ 1200.00
  • Chem-Impex
  • Nα-Fmoc-Nε-isopropyl-Nε-tert-butyloxycarbonyl-L-lysine,≥99%(HPLC) ≥99%(HPLC)
  • 5G
  • $ 541.63
Total 79 raw suppliers
Chemical Property of FMOC-LYS(BOC)(ISOPROPYL)-OH Edit
Chemical Property:
  • Boiling Point:677.1±55.0 °C(Predicted) 
  • PKA:3.88±0.21(Predicted) 
  • PSA:105.17000 
  • Density:1.172±0.06 g/cm3(Predicted) 
  • LogP:6.18500 
  • Storage Temp.:-15°C 
Purity/Quality:

99% *data from raw suppliers

Fmoc-l-lys(boc,ipr)-oh *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of FMOC-LYS(BOC)(ISOPROPYL)-OH

There total 3 articles about FMOC-LYS(BOC)(ISOPROPYL)-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:
With sodium carbonate; In tert-butyl alcohol; at 20 ℃;
Guidance literature:
Multi-step reaction with 3 steps
1: trifluoroacetic acid / dichloromethane / 20 °C
2: trifluoroacetic acid / methanol / 2 h / 20 °C
3: sodium carbonate / tert-butyl alcohol / 20 °C
With sodium carbonate; trifluoroacetic acid; In methanol; dichloromethane; tert-butyl alcohol;
Guidance literature:
Multi-step reaction with 2 steps
1: trifluoroacetic acid / methanol / 2 h / 20 °C
2: sodium carbonate / tert-butyl alcohol / 20 °C
With sodium carbonate; trifluoroacetic acid; In methanol; tert-butyl alcohol;
Refernces Edit
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