Benzyl(dioctyl)oxo-lambda~5~-phosphane

Base Information

• Chemical Name: Benzyl(dioctyl)oxo-lambda~5~-phosphane
• CAS No.: 35794-29-7
• Molecular Formula: C23H41OP
• Molecular Weight: 364.552
• DSSTox Substance ID: DTXSID60517806
• Nikkaji Number: J1.146.666D
• Wikidata: Q82379997
• Mol file: 35794-29-7.mol

Synonyms:benzyl dioctyl phosphine oxide;35794-29-7;Benzyl(dioctyl)oxo-lambda~5~-phosphane;SCHEMBL2991974;DTXSID60517806

Chemical Property of Benzyl(dioctyl)oxo-lambda~5~-phosphane

Chemical Property:

• XLogP3: 7.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 16
• Exact Mass: 364.28950292
• Heavy Atom Count: 25
• Complexity: 313

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCP(=O)(CCCCCCCC)CC1=CC=CC=C1
• Use Description: Phosphine oxide, dioctyl(phenylmethyl)-, a specific chemical compound, serves varied functions across diverse fields. In the realm of polymer chemistry, it acts as a crucial component in the formulation of flame-retardant materials, contributing to enhancing fire resistance in plastics, textiles, and coatings. In the field of organic synthesis, this compound serves as a building block, enabling the creation of complex molecules for medicinal and materials research. Moreover, in the domain of analytical chemistry, it may be employed as a reagent for determining metal ions and other compounds in samples. The compound's multifaceted applications in polymer chemistry, organic synthesis, and analytical chemistry underscore its importance in driving innovation, safety, and research across these distinct scientific domains.

Technology Process of Benzyl(dioctyl)oxo-lambda~5~-phosphane

There total 2 articles about Benzyl(dioctyl)oxo-lambda~5~-phosphane 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: 100.0%

oxyde de dioctyl phosphine (3011-82-3) + benzyl chloride (100-44-7) → benzyl dioctyl phosphine oxide (35794-29-7)

Guidance literature:

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In toluene; at 65 ℃; for 3h; Product distribution; preparation of unsymmetrical tertiary phosphine oxides with chloromethylated compounds; half lives with different phase transfer catalysts;

Reference yield:

→ benzyl dioctyl phosphine oxide (35794-29-7)

Guidance literature:

upstream raw materials:

oxyde de dioctyl phosphine

benzyl chloride

Refernces

• 1、 -. "Preparation of epoxides from olefins using bis(triorganosilyl) peroxides in the presence of activators based on metallic acid derivatives". . . Retrieved 2008/06/13.
• 2、 N'Guyen, Thanh Dung,Boileau, Sylvie,Gautier, Jean-Claude. "Phase transfer catalysis in the chemical modification of polymers. Part III. Preparation of unsymmetrical tertiary phosphine oxides(1)". . p. 288 - 290. Retrieved 2007/10/02.