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Fmoc-DL-Asu-OH

Base Information Edit
  • Chemical Name:Fmoc-DL-Asu-OH
  • CAS No.:1208999-99-8
  • Molecular Formula:C23H25NO6
  • Molecular Weight:411.455
  • Hs Code.:
  • Mol file:1208999-99-8.mol
Fmoc-DL-Asu-OH

Synonyms:Fmoc-DL-Asu-OH

Suppliers and Price of Fmoc-DL-Asu-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
  • Matrix Scientific
  • Fmoc-DL-Asu-OH
  • 5g
  • $ 1169.00
  • Matrix Scientific
  • Fmoc-DL-Asu-OH
  • 1g
  • $ 324.00
  • American Custom Chemicals Corporation
  • FMOC-DL-ASU-OH 95.00%
  • 5G
  • $ 1308.00
  • American Custom Chemicals Corporation
  • FMOC-DL-ASU-OH 95.00%
  • 1G
  • $ 816.00
  • American Custom Chemicals Corporation
  • FMOC-DL-ASU-OH 95.00%
  • 100MG
  • $ 713.79
  • AK Scientific
  • Fmoc-DL-Asu-OH
  • 5g
  • $ 1628.00
Total 5 raw suppliers
Chemical Property of Fmoc-DL-Asu-OH Edit
Chemical Property:
  • Boiling Point:670.9±55.0 °C(Predicted) 
  • PKA:3.89±0.21(Predicted) 
  • PSA:112.93000 
  • Density:1.286±0.06 g/cm3(Predicted) 
  • LogP:4.40430 
Purity/Quality:

99.3% *data from raw suppliers

Fmoc-DL-Asu-OH *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Fmoc-DL-Asu-OH

There total 1 articles about Fmoc-DL-Asu-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:
2-amino-octanedioic acid; With potassium carbonate; In water;
(fluorenylmethoxy)carbonyl chloride; In 1,4-dioxane; water;
Guidance literature:
Multi-step reaction with 2 steps
1: ethyl acetate; dicyclohexyl-carbodiimide / 8 h / 0 °C
2: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 24 h / 20 °C
With ethyl acetate; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In dimethyl sulfoxide;
upstream raw materials:

2-amino-octanedioic acid

(fluorenylmethoxy)carbonyl chloride

Downstream raw materials:

C44H67N13O14S2

Refernces Edit
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