Chemical Properties of Methylphosphonic acid, O-isopropyl-, O-trimethylsilyl-

Methylphosphonic acid, O-isopropyl-, O-trimethylsilyl-

InChI
InChI=1S/C7H19O3PSi/c1-7(2)9-11(3,8)10-12(4,5)6/h7H,1-6H3
InChI Key
SVOLQKHGSREJLY-UHFFFAOYSA-N
Formula
C7H19O3PSi
SMILES
CC(C)OP(C)(=O)O[Si](C)(C)C
Molecular Weight1
210.29
Other Names
  • Methylphosphonic acid, mono-isopropyl ester, TMS
  • Isopropyl trimethylsilyl methylphosphonate
  • IMPA-TBDMS
  • Methylphosphonic acid, isopropyl trimethylsilyl ester
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Physical Properties

Property Value Unit Source
Δvap 54.97 kJ/mol Relay (1.0) Calculated Property
logPoct/wat 3.086 Crippen Calculated Property
Inp [1110.00; 1116.00]   Show Hide
Inp 1116.00 NIST
Inp 1110.00 NIST
Inp 1110.00 NIST
Inp 1116.00 NIST
Inp 1110.00 NIST

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Similar Compounds

O-Ethyl-O'-(trimethyl)silyl methylphosphonate. O-Pinacolyl-O-Trimethylsilyl methylphosphonate. ISOBUTYL METHYLPHOSPHONIC ACID, TMS DERIVATIVE. O-4-Methyl-2-pentyl, methylphosphonic acid, trimethylsilyl ester. Methylphosphonic acid, mono-(3-methyl-1-butyl) ester, TMS. Cyclohexyl-, trimethylsilyl-, ethylphosphonate. Diisopropyl methanephosphonate. Methylphosphonic acid, isobutyl isopropyl ester. Isopropyl methyl methylphosphonate. Methylphosphonic acid, methyl-(2-pentyl) ester. Methylenebis(phosphonic acid), tetraisopropyl ester. Methylphosphonic acid, methyl-(4-methyl-2-pentyl) ester. Methylphosphonic acid, isobutyl pinacolyl ester. Phosphonic acid, methyl, cyclopentyl methyl ester. Bis(tert-butyldimethylsilyl) 3-[(tert-butyldimethylsilyl)amino]propylphosphonate.

Find more compounds similar to Methylphosphonic acid, O-isopropyl-, O-trimethylsilyl-.

Sources

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