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1-Pyrenebutylamine

Base Information
  • Chemical Name:1-Pyrenebutylamine
  • CAS No.:205488-15-9
  • Molecular Formula:C20H19 N
  • Molecular Weight:273.378
  • Hs Code.:2921499090
  • European Community (EC) Number:803-120-9
  • DSSTox Substance ID:DTXSID90391338
  • Nikkaji Number:J1.166.815A
  • Wikidata:Q82188738
  • ChEMBL ID:CHEMBL1474617
  • Mol file:205488-15-9.mol
1-Pyrenebutylamine

Synonyms:1-pyrenebutylamine

Suppliers and Price of 1-Pyrenebutylamine
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
  • TRC
  • 1-Pyrenebutylamine
  • 50mg
  • $ 275.00
  • Crysdot
  • 1-Pyrenebutylamine 95+%
  • 50mg
  • $ 386.00
  • Crysdot
  • 1-Pyrenebutylamine 95+%
  • 250mg
  • $ 1548.00
  • American Custom Chemicals Corporation
  • 1-PYRENEBUTYLAMINE 95.00%
  • 50MG
  • $ 716.10
  • American Custom Chemicals Corporation
  • 1-PYRENEBUTYLAMINE 95.00%
  • 500MG
  • $ 1686.30
  • Alichem
  • 1-(4-Aminobutyl)pyrene
  • 50mg
  • $ 413.40
  • Alichem
  • 1-(4-Aminobutyl)pyrene
  • 250mg
  • $ 1591.20
  • AK Scientific
  • 1-Pyrenebutylamine
  • 50mg
  • $ 601.00
Total 17 raw suppliers
Chemical Property of 1-Pyrenebutylamine
Chemical Property:
  • Melting Point:50-60°C 
  • PSA:26.02000 
  • LogP:5.56570 
  • Storage Temp.:-20°C Freezer 
  • XLogP3:5.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:273.151749610
  • Heavy Atom Count:21
  • Complexity:352
Purity/Quality:

99% *data from raw suppliers

1-Pyrenebutylamine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C3C(=C1)C=CC4=C(C=CC(=C43)C=C2)CCCCN
  • Uses 1-Pyrenebutylamine (cas# 205488-15-9) is a compound useful in organic synthesis.
Technology Process of 1-Pyrenebutylamine

There total 6 articles about 1-Pyrenebutylamine 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 dimethylsulfide borane complex; In tetrahydrofuran; for 1.5h; Heating;
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 48h;
DOI:10.3390/molecules26165032
Guidance literature:
Multi-step reaction with 3 steps
1: oxalyl chloride; DMF / CH2Cl2 / 0.58 h / 20 °C
2: NH3 / CH2Cl2; dioxane / 1.5 h
3: 493 mg / LiAlH4 / tetrahydrofuran / 3 h / 20 °C
With lithium aluminium tetrahydride; oxalyl dichloride; ammonia; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1021/ja057449i
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