1367356-61-3

Basic information

• Product Name: 6-(2-phenylethoxy)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide
• Synonyms: 6-(2-phenylethoxy)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide
• CAS NO: 1367356-61-3
• Molecular Weight: 336.327
• Mol File: 1367356-61-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-(2-phenylethoxy)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(2-phenylethoxy)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide(1367356-61-3)
• EPA Substance Registry System: 6-(2-phenylethoxy)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide(1367356-61-3)

Safety Data

• Hazardous Substances Data: 1367356-61-3(Hazardous Substances Data)

Upstream product

• 60-12-8 2-phenylethanol 
• 35948-25-5 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide 
• 32186-92-8 6-Chloro-6H-dibenz<1,2>oxaphosphorin 

Relevant articles and documents

Synthesis of new organophosphorus compounds using the atherton-todd reaction as a versatile tool

This article discusses the behavior of seven organophosphorus compounds under Atherton-Todd conditions. Therefore, the reactivity and selectivity of different (phen)oxaphosphinines, dioxaphosphinines, dioxaphosphinanes, and diphenylphosphine oxide with three nucleophiles were systematically studied. The results prove the versatility of the Atherton-Todd reaction to a broad range of organophosphorus compounds with different phosphorus environments and reactive Pi-H bonds. The nucleophiles studied in this article were chosen as model substrates for amines and alcohols. Because organophosphorus molecules are important and versatile compounds, for a broad field of applications, novel synthetic approaches are of interest to both academia and industry. As an example, the single-step synthesis of the bridged 1,3-phenylene bis(diphenylphosphinate) with potential flame-retardant properties was added to this study. In addition, the reaction is utilized for the synthesis of a novel organophosphorus anhydride.