78089-65-3

Basic information

• Product Name: methylphosphinyl chloride
• Synonyms: methylphosphinyl chloride
• CAS NO: 78089-65-3
• Molecular Weight: 223.039
• Mol File: 78089-65-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methylphosphinyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: methylphosphinyl chloride(78089-65-3)
• EPA Substance Registry System: methylphosphinyl chloride(78089-65-3)

Safety Data

• Hazardous Substances Data: 78089-65-3(Hazardous Substances Data)

Upstream product

• 615-37-2 ortho-methylphenyl iodide 
• 61820-30-2 ethyl methyl-o-tolylphosphinate 
• 75777-30-9 1-methyl-1,3-dihydro-2,1-benzoxaphosphole 1-oxide 
• 78089-64-2 Methyl(2-tolyl)phosphinyl Chloride 

Downstream Products

• 78089-73-3 P-(α-Chloro-2-tolyl)-P-methylphosphinamide 
• 78108-46-0 N-(4-Phenoxyphenyl)-P-(α-chloro-2-tolyl)-P-methylphosphinamide 
• 78089-54-0 1-Methyl-2-(4-bromophenyl)-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-51-7 1-Methyl-2-(4-methoxyphenyl)-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-52-8 1-Methyl-2-(3,4-dichlorophenyl)-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-57-3 1-Methyl-2-(2-methoxyphenyl)-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-53-9 1-Methyl-2-<3-(trifluoromethyl)phenyl>-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-56-2 1-Methyl-2-(4-phenoxyphenyl)-2,3-dihydro-1H-2,1-benzazaphosphole 1-Oxide 
• 78089-71-1 N-(4-Bromophenyl)-P-(α-chloro-2-tolyl)-P-methylphosphinamide 
• 78089-69-7 N-(3,4-Dichlorophenyl)-P-(α-chloro-2-tolyl)-P-methylphosphinamide 
• 78089-67-5 N-Phenyl-P-(α-chloro-2-tolyl)-P-methylphosphinamide 
• 78089-68-6 N-(4-Methoxyphenyl)-P-(α-chloro-2-tolyl)-P-methylphosphinamide 
• 78089-70-0 N-<3-(Trifluoromethyl)phenyl>-P-(α-chloro-2-tolyl)-P-methylphosphinamide 

Relevant articles and documents

Synthesis of Novel Phosphorus Heterocycles: 1,3-Dihydro-2,1-Benzoxaphosphole 1-Oxides

A class of novel phosphorus heterocycles, 1,3-dihydro-2,1-benzoxaphosphole 1-oxides, has been prepared by two different routes.One general approach involves the cyclization of ortho-substituted phenylphosphinic acid derivatives under either thermal or sol