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3-Naphthalen-1-yl-phenylamine

Base Information
  • Chemical Name:3-Naphthalen-1-yl-phenylamine
  • CAS No.:728919-25-3
  • Molecular Formula:C16H13N
  • Molecular Weight:219.286
  • Hs Code.:
  • DSSTox Substance ID:DTXSID001308289
  • Mol file:728919-25-3.mol
3-Naphthalen-1-yl-phenylamine

Synonyms:728919-25-3;3-naphthalen-1-yl-phenylamine;3-(NAPHTHALEN-1-YL)ANILINE;1-(3-Aminophenyl)naphthalene;3-(1-Naphthalenyl)benzenamine;3-naphthalen-1-ylaniline;3-(1-naphthyl)aniline;3-naphthalen-1-ylphenylamine;SCHEMBL6360162;DTXSID001308289;AKOS005821290;AS-84715;E77791;Z732776172

Suppliers and Price of 3-Naphthalen-1-yl-phenylamine
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
  • Alichem
  • 1-(3-Aminophenyl)naphthalene
  • 1g
  • $ 1701.85
  • Alichem
  • 1-(3-Aminophenyl)naphthalene
  • 500mg
  • $ 1078.00
  • Alichem
  • 1-(3-Aminophenyl)naphthalene
  • 250mg
  • $ 673.20
  • AHH
  • 3-Naphthalen-1-yl-phenylamine 98%
  • 0.5g
  • $ 500.00
Total 15 raw suppliers
Chemical Property of 3-Naphthalen-1-yl-phenylamine
Chemical Property:
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:219.104799419
  • Heavy Atom Count:17
  • Complexity:250
Purity/Quality:

99% *data from raw suppliers

1-(3-Aminophenyl)naphthalene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2C3=CC(=CC=C3)N
Technology Process of 3-Naphthalen-1-yl-phenylamine

There total 10 articles about 3-Naphthalen-1-yl-phenylamine 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 palladium 10% on activated carbon; hydrogen; In ethanol; ethyl acetate; for 5h; under 1551.49 Torr; Inert atmosphere;
DOI:10.1039/c0jm02877k
Guidance literature:
With anhydrous dipotassium phosphate; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); In 1,4-dioxane; at 100 - 110 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201000710
Guidance literature:
With potassium phosphate; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); In 1,4-dioxane; at 110 ℃; Inert atmosphere;
DOI:10.1002/adsc.201100101
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