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(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate

Base Information Edit
  • Chemical Name:(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate
  • CAS No.:1313876-84-4
  • Molecular Formula:C30H41NO4
  • Molecular Weight:479.66
  • Hs Code.:
  • Mol file:1313876-84-4.mol
(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate

Synonyms:(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate

Suppliers and Price of (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate
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
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Total 4 raw suppliers
Chemical Property of (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate

There total 7 articles about (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate 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 potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; for 6h; Product distribution / selectivity; Reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: toluene / 6 h / Reflux; Inert atmosphere
2: potassium carbonate / tetrahydrofuran; N,N-dimethyl-formamide / 20 h / Reflux
With potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; toluene; 2: Wittig reaction;
DOI:10.1007/s00706-011-0582-7
Guidance literature:
Multi-step reaction with 5 steps
1: 1-methyl-pyrrolidin-2-one; iron(III)-acetylacetonate / tetrahydrofuran / 0.75 h / -5 °C / Inert atmosphere
2: potassium borohydride; lithium chloride / tetrahydrofuran / 8 h / Reflux
3: phosphorus tribromide / dichloromethane / 4.3 h / -10 - 20 °C
4: toluene / 6 h / Reflux; Inert atmosphere
5: potassium carbonate / tetrahydrofuran; N,N-dimethyl-formamide / 20 h / Reflux
With 1-methyl-pyrrolidin-2-one; potassium borohydride; iron(III)-acetylacetonate; phosphorus tribromide; potassium carbonate; lithium chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; 5: Wittig reaction;
DOI:10.1007/s00706-011-0582-7
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