Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

C36H38O4

Base Information Edit
C<sub>36</sub>H<sub>38</sub>O<sub>4</sub>

Synonyms:C36H38O4

Suppliers and Price of C36H38O4
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
Total 0 raw suppliers
Chemical Property of C36H38O4 Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C36H38O4

There total 4 articles about C36H38O4 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 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; isopropyl alcohol; at 75 ℃;
DOI:10.1021/ol402017x
Guidance literature:
Multi-step reaction with 3 steps
1.1: diisobutylaluminium hydride / tetrahydrofuran; n-heptane / 4.5 h / 20 °C
1.2: 20 °C
2.1: tetrahydrofuran; diethyl ether / 21 h / -80 °C
3.1: 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran; isopropyl alcohol / 75 °C
With diisobutylaluminium hydride; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; diethyl ether; n-heptane; isopropyl alcohol; 3.1: |Stetter 1,4-Dicarbonyl Synthesis;
DOI:10.1021/ol402017x
Guidance literature:
Multi-step reaction with 2 steps
1: tetrahydrofuran; diethyl ether / 21 h / -80 °C
2: 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran; isopropyl alcohol / 75 °C
With 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; diethyl ether; isopropyl alcohol; 2: |Stetter 1,4-Dicarbonyl Synthesis;
DOI:10.1021/ol402017x
Post RFQ for Price