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3-Aminonaphthalene-1-carbonitrile

Base Information Edit
  • Chemical Name:3-Aminonaphthalene-1-carbonitrile
  • CAS No.:91135-40-9
  • Molecular Formula:C11H8N2
  • Molecular Weight:168.198
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50562921
  • Wikidata:Q82447223
  • Mol file:91135-40-9.mol
3-Aminonaphthalene-1-carbonitrile

Synonyms:3-Aminonaphthalene-1-carbonitrile;91135-40-9;3-Amino-1-naphthonitrile;SCHEMBL10614725;DTXSID50562921

Suppliers and Price of 3-Aminonaphthalene-1-carbonitrile
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
  • 2-Amino-4-cyanonaphthalene
  • 1g
  • $ 1769.25
  • Alichem
  • 2-Amino-4-cyanonaphthalene
  • 500mg
  • $ 950.60
  • Alichem
  • 2-Amino-4-cyanonaphthalene
  • 250mg
  • $ 673.20
Total 1 raw suppliers
Chemical Property of 3-Aminonaphthalene-1-carbonitrile Edit
Chemical Property:
  • PSA:49.81000 
  • LogP:2.87488 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:168.068748264
  • Heavy Atom Count:13
  • Complexity:228
Purity/Quality:

97% *data from raw suppliers

2-Amino-4-cyanonaphthalene *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=C(C=C2C#N)N
Technology Process of 3-Aminonaphthalene-1-carbonitrile

There total 3 articles about 3-Aminonaphthalene-1-carbonitrile 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 ammonium hydroxide; water; iron(II) sulfate; for 0.25h; pH=12; Heating;
DOI:10.1135/cccc20000385
Guidance literature:
Multi-step reaction with 2 steps
1.2: 30 percent / Na2HPO2*H2O; H2O; H2SO4 / 72 h
2.1: 31 percent / FeSO4*7H2O; H2ONH4OH / 0.25 h / pH 12 / Heating
With ammonium hydroxide; water; iron(II) sulfate; 1.1: Diazotization / 1.2: Substitution / 2.1: Reduction;
DOI:10.1135/cccc20000385
Guidance literature:
3-Nitro-1-cyan-naphthalin, Fe, AcOH;
DOI:10.1021/ja01503a028
Refernces Edit
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