C₁₂H₁₆O₄

Base Information

Chemical Name:C₁₂H₁₆O₄
CAS No.:1175758-14-1
Molecular Formula:C₁₂H₁₆O₄
Molecular Weight:224.257
Hs Code.:

C<sub>12</sub>H<sub>16</sub>O<sub>4</sub>

Synonyms:

Suppliers and Price of C₁₂H₁₆O₄

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 C₁₂H₁₆O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₂H₁₆O₄

There total 10 articles about C₁₂H₁₆O₄ 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:

: 100-10-7
4-dimethylamino-benzaldehyde

: 1175758-14-1
C₁₂H₁₆O₄

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / methanol; diethyl ether / 18 h / 0 - 20 °C

2: hydrogenchloride / water / 0.5 h / 20 °C

3: lithium hydroxide / water

4: hydrogenchloride; Staphylococcus epidermis D-lactate dehydrogenase; Candida boidinii formate dehydrogenase; ethylenediaminetetraacetic acid; 2-hydroxyethanethiol; ammonium formate; NAD / water / 20 °C / pH 7 / Enzymatic reaction

5: thionyl chloride

With hydrogenchloride; Candida boidinii formate dehydrogenase; thionyl chloride; ethylenediaminetetraacetic acid; Staphylococcus epidermis D-lactate dehydrogenase; NAD; ammonium formate; sodium hydride; 2-hydroxyethanethiol; lithium hydroxide; In methanol; diethyl ether; water;
DOI:10.1002/ejoc.201201506

Reference yield:

: 10031-82-0
4-ethoxybenzaldehyde

: 1175758-14-1
C₁₂H₁₆O₄

Guidance literature:: Multi-step reaction with 6 steps

1: sodium hydride / methanol; diethyl ether / 18 h / 0 - 20 °C

2: hydrogenchloride / water / 0.5 h / 20 °C

3: triethylamine / dichloromethane / 16 h / 0 - 20 °C

4: hydrogen; Rh(I) [(R,R)-Dipamp](COD) / methanol / 96 h / 20 °C / 3750.38 Torr / Inert atmosphere

5: lithium hydroxide / water; tetrahydrofuran

6: thionyl chloride

With hydrogenchloride; thionyl chloride; Rh(I) [(R,R)-Dipamp](COD); hydrogen; sodium hydride; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water;
DOI:10.1002/ejoc.201201506

Reference yield:

: 1431505-77-9
(R)-methyl 3-(4-ethoxyphenyl)-2-(pivaloyloxy)propanoate

: 1175758-14-1
C₁₂H₁₆O₄

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide / water; tetrahydrofuran

2: thionyl chloride

With thionyl chloride; lithium hydroxide; In tetrahydrofuran; water;
DOI:10.1002/ejoc.201201506