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3-Benzyloxy-4-methoxybenzoyl chloride

Base Information
  • Chemical Name:3-Benzyloxy-4-methoxybenzoyl chloride
  • CAS No.:41222-60-0
  • Molecular Formula:C15H13ClO3
  • Molecular Weight:276.719
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90450191
  • Nikkaji Number:J2.577.642I
  • Wikidata:Q82269792
  • Mol file:41222-60-0.mol
3-Benzyloxy-4-methoxybenzoyl chloride

Synonyms:3-benzyloxy-4-methoxybenzoyl chloride;41222-60-0;3-(benzyloxy)-4-methoxybenzoyl chloride;4-methoxy-3-phenylmethoxybenzoyl chloride;SCHEMBL184987;DTXSID90450191;IXCKJOOGPMRIDP-UHFFFAOYSA-N;3-benzyloxy4-methoxy-benzoyl chloride;AKOS025131056;3-benzyloxy-4-methoxy-benzoyl chloride;3-benzyloxy-4-methoxy benzoic acid chloride;3-(Benzyloxy)-4-methoxybenzoic acid chloride

Suppliers and Price of 3-Benzyloxy-4-methoxybenzoyl chloride
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
Total 1 raw suppliers
Chemical Property of 3-Benzyloxy-4-methoxybenzoyl chloride
Chemical Property:
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:276.0553220
  • Heavy Atom Count:19
  • Complexity:289
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)C(=O)Cl)OCC2=CC=CC=C2
Technology Process of 3-Benzyloxy-4-methoxybenzoyl chloride

There total 6 articles about 3-Benzyloxy-4-methoxybenzoyl chloride 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 thionyl chloride; for 2h; Heating / reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / sodium chlorite; sulfamic acid; acetic acid / H2O / 1 h / 20 °C
2: 94 percent / thionyl chloride / toluene / 6 h / 100 °C
With sodium chlorite; thionyl chloride; aminosulfonic acid; acetic acid; In water; toluene;
DOI:10.1016/j.bmc.2006.08.026
Guidance literature:
Multi-step reaction with 3 steps
1: 94 percent / K2CO3; KI / dimethylformamide / 22 h / 65 °C
2: 93 percent / sodium chlorite; sulfamic acid; acetic acid / H2O / 1 h / 20 °C
3: 94 percent / thionyl chloride / toluene / 6 h / 100 °C
With sodium chlorite; thionyl chloride; aminosulfonic acid; potassium carbonate; acetic acid; potassium iodide; In water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmc.2006.08.026
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