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FMOC-9-AMINONONANOIC ACID

Base Information Edit
  • Chemical Name:FMOC-9-AMINONONANOIC ACID
  • CAS No.:212688-52-3
  • Molecular Formula:C24H29 N O4
  • Molecular Weight:395.499
  • Hs Code.:
  • Mol file:212688-52-3.mol
FMOC-9-AMINONONANOIC ACID

Synonyms:FMOC-9-AMINONONANOIC ACID;FMOC-9-ANC-OH;N-(9-FLUORENYLMETHYLOXYCARBONYL)-9-AMINO-NONANOIC ACID

Suppliers and Price of FMOC-9-AMINONONANOIC ACID
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
  • Fmoc-9-aminononanoic acid
  • 1g
  • $ 559.00
  • Crysdot
  • 9-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)nonanoicacid 97%
  • 5g
  • $ 677.00
  • Chem-Impex
  • Fmoc-9-aminononanoicacid,98%(HPLC) 98%(HPLC)
  • 5G
  • $ 728.00
  • Chem-Impex
  • Fmoc-9-aminononanoicacid,98%(HPLC) 98%(HPLC)
  • 1G
  • $ 156.80
  • Chem-Impex
  • Fmoc-9-aminononanoicacid,98%(HPLC) 98%(HPLC)
  • 250MG
  • $ 78.40
  • American Custom Chemicals Corporation
  • FMOC-9-AMINONONANOIC ACID 95.00%
  • 5MG
  • $ 498.20
  • American Custom Chemicals Corporation
  • FMOC-9-AMINONONANOIC ACID 95.00%
  • 250MG
  • $ 584.00
  • AK Scientific
  • Fmoc-9-aminononanoicacid
  • 1g
  • $ 239.00
  • Acrotein
  • 9-(Fmoc-amino)nonanoicacid 97%
  • 0.5g
  • $ 247.50
Total 5 raw suppliers
Chemical Property of FMOC-9-AMINONONANOIC ACID Edit
Chemical Property:
  • Boiling Point:605.7±38.0 °C(Predicted) 
  • PKA:4.78±0.10(Predicted) 
  • PSA:75.63000 
  • Density:1.158±0.06 g/cm3(Predicted) 
  • LogP:5.73130 
  • Storage Temp.:Store at 0°C 
Purity/Quality:

98%Min *data from raw suppliers

Fmoc-9-aminononanoic acid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Description Fmoc-9-aminononanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs and and other conjugation applications. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
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