C₂₀H₂₄O₄

Base Information

Chemical Name:C₂₀H₂₄O₄
CAS No.:1449419-23-1
Molecular Formula:C₂₀H₂₄O₄
Molecular Weight:328.408
Hs Code.:

C<sub>20</sub>H<sub>24</sub>O<sub>4</sub>

Synonyms:C₂₀H₂₄O₄

Suppliers and Price of C₂₀H₂₄O₄

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 C₂₀H₂₄O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₀H₂₄O₄

There total 6 articles about C₂₀H₂₄O₄ 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: 87.0%

: 1449419-22-0
C₂₃H₃₀O₃S₂

: 1449419-23-1
C₂₀H₂₄O₄

Guidance literature:: With sodium hydrogencarbonate; methyl iodide; In water; acetonitrile; at 20 ℃; for 19h;
DOI:10.1016/j.tet.2013.02.008

Reference yield:

: 1449419-17-3
C₁₅H₂₀O₃S₂

: 1449419-23-1
C₂₀H₂₄O₄

Guidance literature:: Multi-step reaction with 6 steps

1.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -78 °C

1.2: 2.5 h / 0 - 20 °C

2.1: magnesium bromide ethyl etherate / dichloromethane / 1 h / -78 °C

2.2: 1.5 h / -78 °C

3.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran; toluene / 21 h / 0 - 20 °C

4.1: sodium hydroxide / tetrahydrofuran; water; methanol / 12 h / 0 - 20 °C

5.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C

5.2: 21.5 h / 0 - 20 °C

6.1: sodium hydrogencarbonate; methyl iodide / acetonitrile; water / 19 h / 20 °C

With di-isopropyl azodicarboxylate; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; magnesium bromide ethyl etherate; triphenylphosphine; sodium hydroxide; methyl iodide; In tetrahydrofuran; methanol; dichloromethane; water; toluene; acetonitrile; mineral oil; 2.2: |Grignard Reaction / 3.1: |Mitsunobu Displacement;
DOI:10.1016/j.tet.2013.02.008

Reference yield:

: 1449419-19-5
C₁₆H₂₄O₃S₂

: 1449419-23-1
C₂₀H₂₄O₄

Guidance literature:: Multi-step reaction with 4 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran; toluene / 21 h / 0 - 20 °C

2.1: sodium hydroxide / tetrahydrofuran; water; methanol / 12 h / 0 - 20 °C

3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C

3.2: 21.5 h / 0 - 20 °C

4.1: sodium hydrogencarbonate; methyl iodide / acetonitrile; water / 19 h / 20 °C

With di-isopropyl azodicarboxylate; sodium hydride; sodium hydrogencarbonate; triphenylphosphine; sodium hydroxide; methyl iodide; In tetrahydrofuran; methanol; water; toluene; acetonitrile; mineral oil; 1.1: |Mitsunobu Displacement;
DOI:10.1016/j.tet.2013.02.008