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2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE

Base Information Edit
  • Chemical Name:2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE
  • CAS No.:361393-65-9
  • Molecular Formula:C9H11NO
  • Molecular Weight:149.19000
  • Hs Code.:
  • Mol file:361393-65-9.mol
2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE

Synonyms:2,3-dihydro-1-benzofuran-7-ylmethylamine;

Suppliers and Price of 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE
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
  • TRC
  • 2,3-dihydro-1-benzofuran-7-ylmethylamine
  • 250mg
  • $ 265.00
  • TRC
  • 2,3-dihydro-1-benzofuran-7-ylmethylamine
  • 50mg
  • $ 65.00
  • American Custom Chemicals Corporation
  • 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE 95.00%
  • 1G
  • $ 921.69
  • American Custom Chemicals Corporation
  • 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE 95.00%
  • 250MG
  • $ 732.50
Total 5 raw suppliers
Chemical Property of 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE Edit
Chemical Property:
  • PSA:35.25000 
  • LogP:1.78050 
Purity/Quality:

99% *data from raw suppliers

2,3-dihydro-1-benzofuran-7-ylmethylamine *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE

There total 10 articles about 2,3-DIHYDRO-1-BENZOFURAN-7-YLMETHYLAMINE 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:
7-(azidomethyl)-2,3-dihydro-1-benzofuran; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 1.5h;
With sodium hydroxide; water;
With hydrogenchloride; potassium carbonate; more than 3 stages;
Guidance literature:
With ammonium hydroxide; sodium hydroxide; sodium borohydrid; iodine; In tetrahydrofuran; methanol; tert-butyl methyl ether;
Guidance literature:
Multi-step reaction with 3 steps
1: carbon tetrabromide; triphenylphosphine / dichloromethane / 22 °C
2: sodium azide / N,N-dimethyl-formamide / 22 °C
3: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C
With lithium aluminium tetrahydride; sodium azide; carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.04.024
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