C₃₂H₂₅P

Base Information

Chemical Name:C₃₂H₂₅P
CAS No.:2749557-19-3
Molecular Formula:C₃₂H₂₅P
Molecular Weight:440.524
Hs Code.:

Synonyms:

Suppliers and Price of C₃₂H₂₅P

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of C₃₂H₂₅P

Chemical Property:

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

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Technology Process of C₃₂H₂₅P

There total 6 articles about C₃₂H₂₅P 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%

: (M)-(3',4'-dihydro-[1,1'-binaphthalen]-2-yl)diphenylphosphine oxide

: 2749557-19-3
C₃₂H₂₅P

Guidance literature:: (M)-(3',4'-dihydro-[1,1'-binaphthalen]-2-yl)diphenylphosphine oxide; With oxalyl dichloride; In dichloromethane; at 20 ℃; for 0.5h;

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 3.5h;
DOI:10.1002/anie.201509571

Reference yield:

: 1589518-11-5
(1-bromonaphthalen-2-yl)diphenylphosphine oxide

: 2749557-19-3
C₃₂H₂₅P

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium diacetate; lithium tert-butoxide; C₃₅H₃₂F₄NO₄P / 1,4-dioxane / 24 h / 50 °C / Schlenk technique; Inert atmosphere

2.1: oxalyl dichloride / dichloromethane / 0.5 h / 20 °C

2.2: 3.5 h / 0 - 20 °C

With oxalyl dichloride; C₃₅H₃₂F₄NO₄P; palladium diacetate; lithium tert-butoxide; In 1,4-dioxane; dichloromethane;
DOI:10.1002/anie.201509571

Reference yield:

: 17336-59-3
1-tetralone tosylhydrazone

: 2749557-19-3
C₃₂H₂₅P

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium diacetate; lithium tert-butoxide; C₃₅H₃₂F₄NO₄P / 1,4-dioxane / 24 h / 50 °C / Schlenk technique; Inert atmosphere

2.1: oxalyl dichloride / dichloromethane / 0.5 h / 20 °C

2.2: 3.5 h / 0 - 20 °C

With oxalyl dichloride; C₃₅H₃₂F₄NO₄P; palladium diacetate; lithium tert-butoxide; In 1,4-dioxane; dichloromethane;
DOI:10.1002/anie.201509571