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2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol

Base Information Edit
  • Chemical Name:2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol
  • CAS No.:152955-28-7
  • Molecular Formula:C16H18O3
  • Molecular Weight:258.317
  • Hs Code.:2909500000
  • Mol file:152955-28-7.mol
2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol

Synonyms:2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol

Suppliers and Price of 2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol
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
  • Crysdot
  • 2-(3-Hydroxy-2-phenylpropyl)-5-methoxyphenol 95+%
  • 1g
  • $ 698.00
  • Chemenu
  • 2-(3-Hydroxy-2-phenylpropyl)-5-methoxyphenol 95%
  • 1g
  • $ 659.00
  • Alichem
  • 2-(3-Hydroxy-2-phenylpropyl)-5-methoxyphenol
  • 1g
  • $ 573.68
Total 2 raw suppliers
Chemical Property of 2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol Edit
Chemical Property:
  • PSA:49.69000 
  • LogP:2.71940 
Purity/Quality:

≥99% *data from raw suppliers

2-(3-Hydroxy-2-phenylpropyl)-5-methoxyphenol 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol

There total 8 articles about 2-(3-Hydroxy-2-phenylpropyl)-5-Methoxyphenol 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:
Multi-step reaction with 5 steps
1: 96 percent / NaBH4 / tetrahydrofuran; ethanol / 0.75 h / Ambient temperature
2: 70 percent / LiBr, 2,6-lutidine, methanesulfonic anhydride / tetrahydrofuran / 30 h / Ambient temperature
3: 45 percent / n-BuLi, isopropylcyclohexylamine, HMPA / tetrahydrofuran; hexane / 0.25 h / -78 °C
4: 50 percent / LiAlH4 / diethyl ether / 0.5 h / Ambient temperature
5: 3 N HCl / methanol / 1 h / Heating
With 2,6-dimethylpyridine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; lithium aluminium tetrahydride; n-butyllithium; N-cyclohexylisopropylamine; lithium bromide; Methanesulfonic anhydride; In tetrahydrofuran; methanol; diethyl ether; ethanol; hexane;
DOI:10.3987/com-98-8149
Guidance literature:
Multi-step reaction with 2 steps
1: 50 percent / LiAlH4 / diethyl ether / 0.5 h / Ambient temperature
2: 3 N HCl / methanol / 1 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; In methanol; diethyl ether;
DOI:10.3987/com-98-8149
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