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2-Amino-3-hydroxybenzyl alcohol

Base Information Edit
  • Chemical Name:2-Amino-3-hydroxybenzyl alcohol
  • CAS No.:18274-82-3
  • Molecular Formula:C7H9NO2
  • Molecular Weight:139.154
  • Hs Code.:2922509090
  • Mol file:18274-82-3.mol
2-Amino-3-hydroxybenzyl alcohol

Synonyms:2-Amino-3-hydroxybenzyl alcohol;2-amino-3-(hydroxymethyl)phenol

Suppliers and Price of 2-Amino-3-hydroxybenzyl alcohol
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
  • Chemcia Scientific
  • 2-Amino-3-hydroxymethyl-phenol 95%
  • 1 G
  • $ 395.00
  • AK Scientific
  • 2-Amino-3-(hydroxymethyl)phenol
  • 10g
  • $ 3246.00
  • AK Scientific
  • 2-Amino-3-(hydroxymethyl)phenol
  • 5g
  • $ 2222.00
  • AK Scientific
  • 2-Amino-3-(hydroxymethyl)phenol
  • 1g
  • $ 831.00
  • AK Scientific
  • 2-Amino-3-(hydroxymethyl)phenol
  • 100mg
  • $ 310.00
Total 0 raw suppliers
Chemical Property of 2-Amino-3-hydroxybenzyl alcohol Edit
Chemical Property:
  • PSA:66.48000 
  • LogP:1.04790 
Purity/Quality:

2-Amino-3-hydroxymethyl-phenol 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-Amino-3-hydroxybenzyl alcohol

There total 10 articles about 2-Amino-3-hydroxybenzyl alcohol 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 on activated charcoal; hydrogen;
DOI:10.1039/c3ra41080c
Guidance literature:
With sodium tetrahydroborate; C54H50Cl2N2O3Ru2; In ethanol; at 20 ℃; for 3h;
DOI:10.1016/j.jorganchem.2019.120984
Guidance literature:
Multi-step reaction with 5 steps
1: potassium carbonate / acetone
2: nitric acid / 20 °C
3: aluminum (III) chloride / dichloromethane
4: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C
5: hydrogen; palladium on activated charcoal
With aluminum (III) chloride; lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; nitric acid; potassium carbonate; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1039/c3ra41080c
Refernces Edit
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