C₂₅H₄₁O₈P

Base Information

Chemical Name:C₂₅H₄₁O₈P
CAS No.:1393110-95-6
Molecular Formula:C₂₅H₄₁O₈P
Molecular Weight:500.569
Hs Code.:

C<sub>25</sub>H<sub>41</sub>O<sub>8</sub>P

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₅H₄₁O₈P

Chemical Property:

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Technology Process of C₂₅H₄₁O₈P

There total 6 articles about C₂₅H₄₁O₈P 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:

: 5927-18-4
trimethyl phosphonoacetate

: 1393110-95-6
C₂₅H₄₁O₈P

Guidance literature:: Multi-step reaction with 2 steps

1: 4-toluenesulfonyl azide; sodium hydride / tetrahydrofuran; mineral oil / 3 h / 0 - 20 °C

2: rhodium (II) octanoate dimer / dichloromethane / 1 h / 85 °C / Inert atmosphere

With 4-toluenesulfonyl azide; rhodium (II) octanoate dimer; sodium hydride; In tetrahydrofuran; dichloromethane; mineral oil;
DOI:10.1021/ol3017676

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 1393110-95-6
C₂₅H₄₁O₈P

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran; dimethyl sulfoxide; mineral oil / 1 h / 0 °C

1.2: 21 h / 0 - 20 °C

2.1: pyridine; sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 6 h / 0 - 20 °C

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 22 h / 0 - 20 °C

4.1: diisobutylaluminium hydride / tetrahydrofuran; dichloromethane / 1.5 h / -78 °C

5.1: rhodium (II) octanoate dimer / dichloromethane / 1 h / 85 °C / Inert atmosphere

With pyridine; rhodium (II) octanoate dimer; sulfur trioxide pyridine complex; sodium hydride; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; lithium chloride; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; acetonitrile; mineral oil; 2.1: Parikh-Doering oxidation;
DOI:10.1021/ol3017676

Reference yield:

: 1393110-59-2
10-((4-methoxybenzyl)oxy)decanal

: 1393110-95-6
C₂₅H₄₁O₈P

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 22 h / 0 - 20 °C

2: diisobutylaluminium hydride / tetrahydrofuran; dichloromethane / 1.5 h / -78 °C

3: rhodium (II) octanoate dimer / dichloromethane / 1 h / 85 °C / Inert atmosphere

With rhodium (II) octanoate dimer; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/ol3017676