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1-Naphthylhydroxylamine

Base Information Edit
  • Chemical Name:1-Naphthylhydroxylamine
  • CAS No.:607-30-7
  • Molecular Formula:C10H9 N O
  • Molecular Weight:159.188
  • Hs Code.:2928000090
  • UNII:5O045G232P
  • DSSTox Substance ID:DTXSID40209510
  • Nikkaji Number:J2.985H
  • Wikidata:Q26840867
  • Metabolomics Workbench ID:55041
  • ChEMBL ID:CHEMBL261899
  • Mol file:607-30-7.mol
1-Naphthylhydroxylamine

Synonyms:1-naphthylhydroxylamine;N-hydroxy-1-naphthylamine

Suppliers and Price of 1-Naphthylhydroxylamine
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
  • American Custom Chemicals Corporation
  • N-HYDROXY-1-NAPHTHYLAMINE 95.00%
  • 5MG
  • $ 495.66
Total 7 raw suppliers
Chemical Property of 1-Naphthylhydroxylamine Edit
Chemical Property:
  • Vapor Pressure:3.47E-05mmHg at 25°C 
  • Melting Point:79°C 
  • Refractive Index:1.5460 (estimate) 
  • Boiling Point:339.8°C at 760 mmHg 
  • PKA:9.00±0.30(Predicted) 
  • Flash Point:174.9°C 
  • PSA:32.26000 
  • Density:1.283g/cm3 
  • LogP:2.71390 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:159.068413911
  • Heavy Atom Count:12
  • Complexity:149
Purity/Quality:

98%min *data from raw suppliers

N-HYDROXY-1-NAPHTHYLAMINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:Nitrogen Compounds -> Naphthylamines
  • Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2NO
Technology Process of 1-Naphthylhydroxylamine

There total 2 articles about 1-Naphthylhydroxylamine 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 tetrahydroborate; palladium diacetate; In ethanol; dichloromethane; water; at 20 ℃; for 0.0666667h;
DOI:10.1039/c9gc03957k
Guidance literature:
With iron(II) phthalocyanine; In toluene; regioselective reaction; Reflux; Inert atmosphere;
DOI:10.1016/j.tet.2009.03.004
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