308820-90-8

Basic information

• Product Name: benzyl phenyl-H-phosphinate
• Synonyms: benzyl phenyl-H-phosphinate
• CAS NO: 308820-90-8
• Molecular Weight: 232.219
• Mol File: 308820-90-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: benzyl phenyl-H-phosphinate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl phenyl-H-phosphinate(308820-90-8)
• EPA Substance Registry System: benzyl phenyl-H-phosphinate(308820-90-8)

Safety Data

• Hazardous Substances Data: 308820-90-8(Hazardous Substances Data)

Upstream product

• 644-97-3 Dichlorophenylphosphine 
• 100-51-6 benzyl alcohol 
• 1779-48-2 phenylphosphinic acid 
• 501-53-1 benzyl chloroformate 
• 100-39-0 benzyl bromide 
• 172487-18-2 ethyl Phenylphosphinate 
• 52744-21-5 phenyl phenylphosphinate 

Downstream Products

• 1188298-12-5 phenylmetyl N,P-diphenylphosphonamidate 
• 106019-42-5 Phenyl-phosphonic acid monobenzyl ester; compound with adamantan-1-ylamine 
• 1027325-04-7 2-(benzyloxy-phenyl-phosphinoylmethyl)-pentanedioic acid dibenzyl ester 
• 19236-48-7 monobenzyl phenylphosphonate 

Relevant articles and documents

Palladium-Catalyzed Domino Cyclization/Phosphorylation of gem-Dibromoolefins with P(O)H Compounds: Synthesis of Phosphorylated Heteroaromatics

We presented a palladium-catalyzed domino cyclization/phosphorylation of gem-dibromoolefins, which utilize H-phosphinates and secondary phosphine oxides as the phosphine sources, respectively. A variety of phosphorylated heteroaromatics were obtained in m

Continuous flow esterification of a H-phosphinic acid, and transesterification of H-phosphinates and H-phosphonates under microwave conditions

The microwave (MW)-assisted direct esterification of phenyl-H-phosphinic acid, transesterification of the alkyl phenyl-H-phosphinates so obtained, and the similar reaction of dibenzyl phosphite (DBP) were investigated in detail, and the batch accomplishme

Silver-promoted cascade radical cyclization of γ,δ-unsaturated oxime esters with P(O)H compounds: synthesis of phosphorylated pyrrolines

A cascade radical cyclization was realized for the first silver-promoted imino-phosphorylation of γ,δ-unsaturated oxime esters, which provided a step-economical and redox-neutral route to access a variety of phosphorylated pyrrolines in good to excellent yields. Moreover, a new bulky trivalent phosphine ligand with a pyrroline motif was obtained through a deoxidation process.