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(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid

Base Information
  • Chemical Name:(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid
  • CAS No.:1007096-37-8
  • Molecular Formula:C28H28N2O5
  • Molecular Weight:472.541
  • Hs Code.:
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid

Synonyms:(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid

Suppliers and Price of (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid
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
  • Iris Biotech GmbH
  • Fmoc-L-Lys(Bz)-OH
  • 5 g
  • $ 3699.00
  • American Custom Chemicals Corporation
  • FMOC-LYS(BZO)-OH 95.00%
  • 5MG
  • $ 498.20
Total 3 raw suppliers
Chemical Property of (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Fmoc-L-Lys(Bz)-OH *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid

There total 3 articles about (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoic acid 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:
(S)-methyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-benzamidohexanoate; With water; calcium chloride; sodium hydroxide; In isopropyl alcohol; at 20 ℃; for 5h;
With acetic acid; In water; isopropyl alcohol;
DOI:10.1016/j.bmc.2010.06.035
Guidance literature:
Multi-step reaction with 2 steps
1: dicyclohexyl-carbodiimide / N,N-dimethyl-formamide / 12 h / 0 - 20 °C / Inert atmosphere
2: sodium hydrogencarbonate / dichloromethane / 24 h / 20 °C
With sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;
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