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5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid

Base Information Edit
  • Chemical Name:5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid
  • CAS No.:123622-48-0
  • Molecular Formula:C20H21NO4
  • Molecular Weight:339.391
  • Hs Code.:29242990
  • European Community (EC) Number:832-970-3
  • Mol file:123622-48-0.mol
5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid

Synonyms:123622-48-0;Fmoc-5-Ava-OH;Fmoc-5-aminopentanoic acid;5-(Fmoc-amino)valeric acid;5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid;5-(Fmoc-amino)pentanoic acid;Pentanoic acid, 5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-;Fmoc-5-aminopentanoic acid, tech grade;5-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic Acid;MFCD00235889;Fmoc-5-Ava-OH Fmoc-5-aminopentanoic acid;N-(9-FLUORENYLMETHYLOXYCARBONYL)-5-AMINO-PENTANOIC ACID;5-({[(9H-FLUOREN-9-YL)METHOXY]CARBONYL}AMINO)PENTANOIC ACID;Fmoc-Ape(5)-OH;SCHEMBL97174;N-Fmoc-5-aminopentanoic acid;FMOC-5-AMINOPENTANOICACID;AC1980;AKOS013376082;CS-W009834;AS-70962;BP-28255;SY066349;Fmoc-5-Ava-OH, >=98.0% (HPLC);FT-0679730;EN300-81114;A890666;J-004964;N-(9-fluorenylmethoxycarbonyl)-5-amino-pentanoic acid;5-(((9H-fluoren-9-yl)methoxy)carbonylamino)pentanoic acid

Suppliers and Price of 5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic 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-5-aminovaleric acid
  • 2g
  • $ 333.00
  • Usbiological
  • Fmoc-5-aminopentanoic acid, tech grade
  • 100mg
  • $ 305.00
  • TRC
  • Fmoc-5-aminopentanoicacid(TechnicalGrade)
  • 500mg
  • $ 65.00
  • Sigma-Aldrich
  • Fmoc-5-Ava-OH ≥98.0% (HPLC)
  • 1g
  • $ 48.30
  • Sigma-Aldrich
  • Fmoc-5-Ava-OH ≥98.0% (HPLC)
  • 5g
  • $ 174.00
  • Matrix Scientific
  • Fmoc-5-aminopentanoic acid 95%
  • 25g
  • $ 399.00
  • Matrix Scientific
  • Fmoc-5-aminopentanoic acid 95%
  • 5g
  • $ 99.00
  • Iris Biotech GmbH
  • Fmoc-5-Ava-OH
  • 5 g
  • $ 236.25
  • Iris Biotech GmbH
  • Fmoc-5-Ava-OH
  • 1 g
  • $ 67.50
  • Frontier Specialty Chemicals
  • Fmoc-5-aminovalericacid 98%
  • 5g
  • $ 339.00
Total 47 raw suppliers
Chemical Property of 5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid Edit
Chemical Property:
  • Melting Point:135-136 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3)) 
  • Boiling Point:562.24 °C at 760 mmHg 
  • PKA:4.71±0.10(Predicted) 
  • Flash Point:293.832 °C 
  • PSA:75.63000 
  • Density:1.231g/cm3 
  • LogP:4.17090 
  • Storage Temp.:2-8°C 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:339.14705815
  • Heavy Atom Count:25
  • Complexity:445
Purity/Quality:

98%,99%, *data from raw suppliers

Fmoc-5-aminovaleric acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCCC(=O)O
  • Description Fmoc-5-aminopentanoic 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. 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.
  • Uses 5-(Fmoc-amino)valeric acid is used as pharmaceutical intermediate. Fmoc-5-aminopentanoic acid, tech grade
Technology Process of 5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid

There total 5 articles about 5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic 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:
With sodium hydrogencarbonate; In 1,4-dioxane; water; at 20 ℃;
DOI:10.1039/c3ob41221k
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