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8-Amino-2-naphthoic acid

Base Information Edit
  • Chemical Name:8-Amino-2-naphthoic acid
  • CAS No.:5043-19-6
  • Molecular Formula:C11H9NO2
  • Molecular Weight:187.198
  • Hs Code.:2922499990
  • European Community (EC) Number:895-223-0
  • DSSTox Substance ID:DTXSID90540925
  • Nikkaji Number:J36.386C
  • Wikidata:Q82417063
  • Mol file:5043-19-6.mol
8-Amino-2-naphthoic acid

Synonyms:8-Amino-2-naphthoic acid;5043-19-6;8-Aminonaphthalene-2-carboxylic acid;SCHEMBL689325;DTXSID90540925;PBWULNOSRHQTHZ-UHFFFAOYSA-N;MFCD18413487;SY273202;EN300-116573

Suppliers and Price of 8-Amino-2-naphthoic 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
  • Alichem
  • 1-Aminonaphthalene-7-carboxylicacid
  • 500mg
  • $ 999.60
  • Alichem
  • 1-Aminonaphthalene-7-carboxylicacid
  • 1g
  • $ 1701.85
  • AK Scientific
  • 8-Amino-2-naphthoicacid
  • 1g
  • $ 1680.00
Total 1 raw suppliers
Chemical Property of 8-Amino-2-naphthoic acid Edit
Chemical Property:
  • PSA:63.32000 
  • LogP:2.70140 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:187.063328530
  • Heavy Atom Count:14
  • Complexity:229
Purity/Quality:

95% *data from raw suppliers

1-Aminonaphthalene-7-carboxylicacid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC2=C(C=C(C=C2)C(=O)O)C(=C1)N
Technology Process of 8-Amino-2-naphthoic acid

There total 8 articles about 8-Amino-2-naphthoic 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:
Multi-step reaction with 2 steps
1: Raney nickel; ethyl acetate; ethanol / Hydrogenation
2: aq.-ethanolic NaOH
With sodium hydroxide; ethanol; nickel; ethyl acetate;
DOI:10.1021/ja01134a055
Guidance literature:
Multi-step reaction with 3 steps
1: (i) aq. H2SO4, AcOH, (ii) /BRN= 1718733/
2: H2 / Raney-Ni / ethanol
3: aq. HCl
With hydrogenchloride; hydrogen; nickel; In ethanol;
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