C₃₇H₄₀O₈

Base Information

Chemical Name:C₃₇H₄₀O₈
CAS No.:1186304-36-8
Molecular Formula:C₃₇H₄₀O₈
Molecular Weight:612.72
Hs Code.:

C<sub>37</sub>H<sub>40</sub>O<sub>8</sub>

Synonyms:C₃₇H₄₀O₈

Suppliers and Price of C₃₇H₄₀O₈

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 0 raw suppliers

Chemical Property of C₃₇H₄₀O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₇H₄₀O₈

There total 15 articles about C₃₇H₄₀O₈ 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:

Reference yield: 95.0%

: 1186304-24-4
C₃₇H₃₈O₈

: 1186304-36-8
C₃₇H₄₀O₈

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; triethylamine; In ethyl acetate; at 20 ℃; for 24h; under 2250.23 Torr;
DOI:10.1055/s-0029-1217510

Reference yield:

: 621-59-0
isovanillin

: 1186304-36-8
C₃₇H₄₀O₈

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetra-N-butylammonium tribromide; orthoformic acid triethyl ester / 6 h / 65 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 165 °C

3.1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 0 - 20 °C

4.1: acetonitrile / 6 h / Reflux

4.2: 12 h / Reflux

5.1: 18-crown-6 ether; potassium carbonate / dichloromethane / 24 h / Reflux

6.1: 5% Pd(II)/C(eggshell); hydrogen; triethylamine / ethyl acetate / 24 h / 20 °C / 2250.23 Torr / Autoclave

With sodium tetrahydroborate; 18-crown-6 ether; 5% Pd(II)/C(eggshell); hydrogen; tetra-N-butylammonium tribromide; potassium carbonate; triethylamine; orthoformic acid triethyl ester; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 5.1: Wittig reaction;
DOI:10.1002/ejoc.201001023

Reference yield:

: 1186304-19-7
4-[5-(1,3-dioxan-2-yl)-2-methoxyphenoxy]benzaldehyde

: 1186304-36-8
C₃₇H₄₀O₈

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 0 - 20 °C

2.1: acetonitrile / 6 h / Reflux

2.2: 12 h / Reflux

3.1: 18-crown-6 ether; potassium carbonate / dichloromethane / 24 h / Reflux

4.1: 5% Pd(II)/C(eggshell); hydrogen; triethylamine / ethyl acetate / 24 h / 20 °C / 2250.23 Torr / Autoclave

With sodium tetrahydroborate; 18-crown-6 ether; 5% Pd(II)/C(eggshell); hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; acetonitrile; 3.1: Wittig reaction;
DOI:10.1002/ejoc.201001023