Chemical Properties of Clorazepate M (hydroxy-), isomer 1, hydrolysis, acetylated

Clorazepate M (hydroxy-), isomer 1, hydrolysis, acetylated

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InChI Key
Molecular Weight1

Physical Properties

Property Value Unit Source
Δf -126.11 kJ/mol Joback Calculated Property
Δfgas -387.79 kJ/mol Joback Calculated Property
Δfus 41.98 kJ/mol Joback Calculated Property
Δvap 93.44 kJ/mol Joback Calculated Property
logPoct/wat 3.45 Crippen Calculated Property
Pc 2300.32 kPa Joback Calculated Property
Tboil 928.29 K Joback Calculated Property
Tc 1170.75 K Joback Calculated Property
Tfus 626.35 K Joback Calculated Property
Vc 0.89 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 664.39 J/mol×K 928.29 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>C=O (nonring) 3
=CH- (ring) 7
=C< (ring) 5
-Cl 1
>NH 1
-CH3 2

Similar Compounds

Nordazepam M (hydroxymethoxy-), hydrolysis, acetylated. Diazepam, M(HO-), acid hydrolyzed, acetylated. Halazepam M (hydroxy-), isomer 2, hydrolysis, acetylated. Clorazepate M (hydroxy-), isomer 2, hydrolysis, acetylated. Halazepam M (hydroxymethoxy-), hydrolysis, acetylated. 4-Chloroacetamidobenzophenone. Ethylloflazepate, hydrolysis, acetylated. Halazepam, hydrolysis. 2-(2-propynylamino)-5-chloro-benzophenone. Flurazepam M (hydroxyethyl-), hydrolysis, acetylated. Clonazepam M (amino-), hydrolysis, acetylated. Flurazepam M (bisdesethyl-)-H2O, hydrolysis, acetylated. 1-Benzoylamino-4-chloro-anthraquinone. Quazepam + M (oxo-), hydrolysis. Buclizine M (hydroxy-chlorobenzophenone), isomer 1, acetylated.

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