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1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE

Base Information
  • Chemical Name:1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE
  • CAS No.:49812-93-3
  • Molecular Formula:C10H13N*ClH
  • Molecular Weight:183.681
  • Hs Code.:
  • Mol file:49812-93-3.mol
1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE

Synonyms:2-Naphthalenamine,1,2,3,4-tetrahydro-, hydrochloride (9CI); 2-Naphthylamine, 1,2,3,4-tetrahydro-,hydrochloride (7CI,8CI); (?à)-2-Aminotetralin hydrochloride; 1,2,3,4-Tetrahydro-2-naphthylaminehydrochloride; NSC 52717

Suppliers and Price of 1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE
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
Total 3 raw suppliers
Chemical Property of 1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE
Chemical Property:
  • PSA:26.02000 
  • LogP:3.00490 
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE

There total 7 articles about 1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE 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 hydrogenchloride; ammonium acetate; sodium cyanoborohydride; In methanol; for 72h; Ambient temperature;
DOI:10.1021/jm00181a009
Guidance literature:
Multi-step reaction with 2 steps
1: 81 percent / L-Selectride / tetrahydrofuran / 1.) -78 deg C, 4 h, 2.) r.t., 30 min
2: 1.) H2, 2.) H2 / 1.) 10percent Pd/C, 2.) Raney-Ni / 1.) MeOH, r.t., 1 h, 2.) r.t., 4 h, 50 bar
With hydrogen; L-Selectride; palladium on activated charcoal; nickel; In tetrahydrofuran;
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) LDA / 1.) THF, hexane, -78 deg C, 1 h, 2.) THF, -78 deg C, 3 min
2: 81 percent / L-Selectride / tetrahydrofuran / 1.) -78 deg C, 4 h, 2.) r.t., 30 min
3: 1.) H2, 2.) H2 / 1.) 10percent Pd/C, 2.) Raney-Ni / 1.) MeOH, r.t., 1 h, 2.) r.t., 4 h, 50 bar
With hydrogen; L-Selectride; lithium diisopropyl amide; palladium on activated charcoal; nickel; In tetrahydrofuran;
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