16391-06-3

Basic information

• Product Name: DIMETHYLPHOSPHINIC ACID
• Synonyms: Methyl-phosphinicacidmethylester
• CAS NO: 16391-06-3
• Molecular Formula: C₂H₇O₂P
• Molecular Weight: 94.049541
• Mol File: 16391-06-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 88.9±23.0 °C(Predicted)
• Appearance: /
• CAS DataBase Reference: DIMETHYLPHOSPHINIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYLPHOSPHINIC ACID(16391-06-3)
• EPA Substance Registry System: DIMETHYLPHOSPHINIC ACID(16391-06-3)

Safety Data

• Hazardous Substances Data: 16391-06-3(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 67-56-1 methanol 
• 88847-59-0 Bis (2-methoxyphenyl) methylphosphonate 
• 138869-16-6 Bis (3-methoxyphenyl) methylphosphonate 
• 60705-73-9 Bis (4-methoxyphenyl) methylphosphonate 

Downstream Products

• 190127-10-7 (1-Benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-methyl-phosphinic acid methyl ester 
• 904702-93-8 C₉H₁₂FO₃P 
• 10580-44-6 dimethyl phenylene-1,4-bis(methyl)phosphinate 
• 132205-80-2 dimethyl phosphonate 

Related news

Gas-phase electron diffraction study of cyclic dimer of DIMETHYLPHOSPHINIC ACID (cas 16391-06-3) (Me2P(O)OH)2 using quantum chemical data and a priori force field08/05/2019

The molecular structure of the hydrogen bonded cyclic dimer of dimethylphosphinic acid (Me2P(O)OH)2 was determined by gas-phase electron diffraction (GED) at 433 K. The presence of monomer cannot be determined at this temperature within the error limits for the GED method. Structural analysis ...detailed

Relevant articles and documents

Photolysis of bis(methoxyphenyl) methylphosphonates. Their emission spectra and formation of dimethoxybiphenyl and dimethoxy-9,10-dioxaanthracene

Upon UV-irradiation in methanol, bis(methoxyphenyl) methylphosphonates underwent an intramolecular coupling of two methoxyphenyl groups to give dimethoxybiphenyls and dimethoxy-9,10-dioxaanthracenes. The reactivities and fluorescence spectra of the phosphonates were sensitive to the position of the methoxy group. These photo-induced couplings proceed probably through the formation of the two types of singlet intramolecular excimers.