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Trimethyl-phosphorthionat, also known as trimethyl phosphite, is an organophosphorus compound with the chemical formula (CH3O)3P. It is a colorless, viscous liquid that is soluble in water and most organic solvents. Trimethyl-phosphorthionat is primarily used as a precursor in the synthesis of various organophosphorus compounds, such as flame retardants, pesticides, and other chemicals. Trimethyl phosphite is also employed as a stabilizer for halogenated hydrocarbons and as a plasticizer for polymers. It is produced industrially through the reaction of phosphorus trichloride with methanol. Due to its potential health and environmental risks, proper handling and disposal procedures are essential when working with trimethyl-phosphorthionat.

55649-26-8

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55649-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55649-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55649-26:
(7*5)+(6*5)+(5*6)+(4*4)+(3*9)+(2*2)+(1*6)=148
148 % 10 = 8
So 55649-26-8 is a valid CAS Registry Number.

55649-26-8Relevant academic research and scientific papers

Properties and Reactions of Trimethyl Phosphite, Trimethyl Phosphate, Triethyl Phosphate, and Trimethyl Phosphorothionate by Ion Cyclotron Resonance Spectroscopy

Hodges, Ronald V.,McDonnell, T. J.,Beauchamp, J. L.

, p. 1327 - 1332 (2007/10/02)

The gas-phase ion-molecule reactions occurring in trimethyl phosphite, trimethyl phosphate, triethyl phosphate, and trimethyl phosphorothionate have been investigated by ion cyclotron resonance spectroscopy.Protonated parent ions, tetracoordinated phosphonium ions, and cluster ions are the reaction products observed.The proton affinities of these compounds have been determined to be 222.9, 214.2, 218.7, and 216.6 kcal/mol, respectively (relative to PA(NH3) = 207.0 kcal/mol).Homolytic bond dissociation energies of the protonated species are calculated using adiabatic ionization potentials determined by photoelectron spectroscopy.The trends in these quantities are discussed.A reasonable value for the correlated homolytic bond dissociation energy of trimethyl phosphite indicates that the first ionization potential of this molecule should be assigned to the phosphorus lone pair.The application of chemical ionization mass spectrometry to the analysis of phosphorus esters is briefly discussed.

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