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2'-Chlorobiphenyl-4-ylamine hydrochloride

Base Information
  • Chemical Name:2'-Chlorobiphenyl-4-ylamine hydrochloride
  • CAS No.:1204-42-8
  • Molecular Formula:C12H10 Cl N
  • Molecular Weight:203.671
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50698133
  • Mol file:1204-42-8.mol
2'-Chlorobiphenyl-4-ylamine hydrochloride

Synonyms:1204-42-8;2'-chlorobiphenyl-4-ylamine hydrochloride;4-(2-chlorophenyl)aniline;hydrochloride;2'-CHLORO-BIPHENYL-4-YLAMINE HYDROCHLORIDE;2/'-CHLORO-BIPHENYL-4-YLAMINE HYDROCHLORIDE;2-Chloro-4'-Aminobiphenyl HCl;2'-chlorobiphenyl-4-ylamine HCl;DTXSID50698133;2'-Chloro[1,1'-biphenyl]-4-amine--hydrogen chloride (1/1)

Suppliers and Price of 2'-Chlorobiphenyl-4-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
  • American Custom Chemicals Corporation
  • 2'-CHLORO-BIPHENYL-4-YLAMINE HYDROCHLORIDE 95.00%
  • 5MG
  • $ 504.69
Total 16 raw suppliers
Chemical Property of 2'-Chlorobiphenyl-4-ylamine hydrochloride
Chemical Property:
  • PSA:26.02000 
  • LogP:4.97240 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:239.0268547
  • Heavy Atom Count:15
  • Complexity:175
Purity/Quality:

98%,99%, *data from raw suppliers

2'-CHLORO-BIPHENYL-4-YLAMINE HYDROCHLORIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)C2=CC=C(C=C2)N)Cl.Cl
Technology Process of 2'-Chlorobiphenyl-4-ylamine hydrochloride

There total 10 articles about 2'-Chlorobiphenyl-4-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 manganese(IV) oxide; In acetonitrile; at 20 ℃; Overall yield = 70 %; regioselective reaction;
DOI:10.1021/jo301980j
Guidance literature:
With palladium diacetate; potassium carbonate; triphenylphosphine; In toluene; for 24h; Inert atmosphere; Reflux;
DOI:10.1021/jm800963t
Guidance literature:
With PPA; trifluoroacetic acid; at 20 ℃; for 3h; Further byproducts. Title compound not separated from byproducts.;
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