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3,4-Dihydro-7-Methoxy-1-naphthol Acetate

Base Information
  • Chemical Name:3,4-Dihydro-7-Methoxy-1-naphthol Acetate
  • CAS No.:20176-04-9
  • Molecular Formula:C13H14O3
  • Molecular Weight:218.252
  • Hs Code.:
  • Mol file:20176-04-9.mol
3,4-Dihydro-7-Methoxy-1-naphthol Acetate

Synonyms:1-Acetoxy-7-methoxy-3.4-dihydro-naphthalin

Suppliers and Price of 3,4-Dihydro-7-Methoxy-1-naphthol Acetate
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
  • Usbiological
  • 3,4-Dihydro-7-methoxy-1-naphthol Acetate
  • 1g
  • $ 460.00
  • TRC
  • 3,4-Dihydro-7-methoxy-1-naphtholAcetate
  • 1g
  • $ 165.00
Total 3 raw suppliers
Chemical Property of 3,4-Dihydro-7-Methoxy-1-naphthol Acetate
Chemical Property:
  • Boiling Point:366.6±41.0 °C(Predicted) 
  • Density:1.15±0.1 g/cm3(Predicted) 
Purity/Quality:

99% *data from raw suppliers

3,4-Dihydro-7-methoxy-1-naphthol Acetate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 3,4-Dihydro-7-methoxy-1-naphthol Acetate, can be used for the enantioselective formation of the 2-Acetoxy-1-tetralones, using a chiral supporting electrolyte.
Technology Process of 3,4-Dihydro-7-Methoxy-1-naphthol Acetate

There total 5 articles about 3,4-Dihydro-7-Methoxy-1-naphthol Acetate 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-Methoxy-1-tetralone; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 2h;
acetic anhydride; In tetrahydrofuran;
DOI:10.1021/acs.orglett.5b01507
Guidance literature:
Multi-step reaction with 2 steps
1: (cyclization)
2: TsOH
With toluene-4-sulfonic acid;
DOI:10.1021/ja01020a027
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