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4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL

Base Information
  • Chemical Name:4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL
  • CAS No.:41032-95-5
  • Molecular Formula:C22H22O3
  • Molecular Weight:334.41
  • Hs Code.:2909309090
  • Mol file:41032-95-5.mol
4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL

Synonyms:4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL

Suppliers and Price of 4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL
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
  • American Custom Chemicals Corporation
  • 4,4'-DIMETHOXY-4'-METHYLTRITYL ALCOHOL 95.00%
  • 0.5G
  • $ 1127.50
  • AHH
  • 4,4-Dimethoxy-4-methyltritylalcohol 95%
  • 5g
  • $ 500.00
Total 5 raw suppliers
Chemical Property of 4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL
Chemical Property:
  • PSA:38.69000 
  • LogP:4.29640 
Purity/Quality:

98%min *data from raw suppliers

4,4'-DIMETHOXY-4'-METHYLTRITYL ALCOHOL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4,4'-DIMETHOXY-4''-METHYLTRITYL ALCOHOL

There total 2 articles about 4,4'-DIMETHOXY-4''-METHYLTRITYL 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:
1-bromo-4-methoxy-benzene; With magnesium; In tetrahydrofuran; at 20 ℃;
4-methyl-benzoic acid methyl ester; In tetrahydrofuran; at 0 - 20 ℃; for 1h;
Guidance literature:
4,4'-Dimethoxybenzophenon, 4-Tolylmagnesiumbromid;
DOI:10.1002/macp.1973.021640105
Guidance literature:
Multi-step reaction with 6 steps
1: acetyl chloride / 1 h / Heating
2: pyridine / 0 °C
3: N-bromosuccinimide; N,N'-azobisisobutyronitrile / CCl4 / 0.33 h / Heating
4: 24 g / N-ethyldiisopropylamine / dimethylformamide / 3 h / 20 °C
5: 62 percent / m-chloroperbenzoic acid; sodium bicarbonate / CH2Cl2 / 0.17 h / 0 °C
6: 97 percent / imidazole / dimethylformamide / 1 h / 20 °C
With pyridine; 1H-imidazole; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; acetyl chloride; 3-chloro-benzenecarboperoxoic acid; In tetrachloromethane; dichloromethane; N,N-dimethyl-formamide;
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