Chemical Properties of 1,3-Propanediol, 2,2-dimethyl-, cyclic phosphorochloridate

1,3-Propanediol, 2,2-dimethyl-, cyclic phosphorochloridate

InChI
InChI=1S/C5H10ClO3P/c1-5(2)3-8-10(6,7)9-4-5/h3-4H2,1-2H3
InChI Key
VZMUCIBBVMLEKC-UHFFFAOYSA-N
Formula
C5H10ClO3P
SMILES
CC1(C)COP(=O)(Cl)OC1
Molecular Weight1
184.56
Other Names
  • 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide
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Physical Properties

Property Value Unit Source
ΔfH°gas -668.73 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 61.15 kJ/mol Relay (1.0) Calculated Property
logPoct/wat 2.406 Crippen Calculated Property
McVol 120.760 ml/mol McGowan Calculated Property
Tboil 508.97 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, 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

1,3-Propanediol, 2,2-dimethyl-, cyclic hydrogen phosphate. 1,3-Propanediol,2,2-dimethyl-, bis(diethylphosphate). 1,3-Propanediol, 2,2-dimethyl-, cyclic 2,2-dichloro-vinyl phosphonate. 1,3-Propanediol, 2,2-dimethyl-, bis(cyclic 2,2-dimethyltrimethylene phosphite). 4-METHYL-2,6,7-TRIOXA-1-PHOSPHABICYCLO [2.2.2] OCTANE. Phosphonic acid, chloro, cyclic 2-ethyl-2-hydroxy-methyltrimethylene ester. 1,3-Propanediol, 2,2-dimethyl-, cyclic chloromethyl phosphonate. 4-Methyl-2,6,7-trioxa-1-phosphabicyclo(2.2.2)octane-1-sulfide. 1,3-Propanediol, 2,2-dimethyl-, bis(cyclic 2,2-dimethyltrimethylene phosphorothionate. 4-Ethyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane 1-oxide. 4-ISOPROPYL-2,6,7-TRIOXA-1-PHOSPHABICYCLO[2.2.2]OCTANE 1-OXIDE. Methylphosphonic acid, methyl neo-pentyl ester. Phosphorochloridic acid, dipropyl ester. 1,3,2-Dioxaphosphorinane, 5,5-dimethyl-2-phenoxy-, 2-oxide. Phosgard 2xc20.

Find more compounds similar to 1,3-Propanediol, 2,2-dimethyl-, cyclic phosphorochloridate.

Sources

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