Chemical Properties of Quazepam + M (oxo-), hydrolysis

Quazepam + M (oxo-), hydrolysis

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InChI
InChI=1S/C15H10ClF4NO/c16-9-5-6-13(21-8-15(18,19)20)11(7-9)14(22)10-3-1-2-4-12(10)17/h1-7,21H,8H2
InChI Key
VGNVFAXJHFXDAT-UHFFFAOYSA-N
Formula
C15H10ClF4NO
SMILES
O=C(c1ccccc1F)c1cc(Cl)ccc1NCC(F)(F)F
Molecular Weight1
331.69
Sources

Physical Properties

Property Value Unit Source
Δf -556.51 kJ/mol Joback Calculated Property
Δfgas -782.32 kJ/mol Joback Calculated Property
Δfus 37.32 kJ/mol Joback Calculated Property
Δvap 68.53 kJ/mol Joback Calculated Property
logPoct/wat 4.68 Crippen Calculated Property
Pc 2137.41 kPa Joback Calculated Property
Tboil 746.22 K Joback Calculated Property
Tc 963.44 K Joback Calculated Property
Tfus 486.50 K Joback Calculated Property
Vc 0.81 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 547.76 J/mol×K 746.22 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-Cl 1
=CH- (ring) 7
=C< (ring) 5
-CH2- 1
-F 4
>C< 1
>NH 1
>C=O (nonring) 1

Similar Compounds

2-Methylamino-5-chloro-2'-fluorobenzophenone. Ethylloflazepate, hydrolysis, acetylated. 5-Chloro-2'-fluoro-2-diethyaminoethylaminobenzophenone. Methanone, (2-amino-5-chlorophenyl)(2-fluorophenyl)-. 2-(2-propynylamino)-5-chloro-benzophenone. Flurazepam M (bisdesethyl-)-H2O, hydrolysis, acetylated. Flurazepam M (hydroxyethyl-), hydrolysis, acetylated. 4-Chloroacetamidobenzophenone. 5-Amino-2'-fluoro-2-methylaminobenzophenone. Clorazepate M (hydroxy-), isomer 2, hydrolysis, acetylated. Flunitrazepam M (amino-), hydrolysis, acetylated. 2-methylamino-5-amino-2'-fluoro-benzophenone, acetylated. Methanone, (2-fluorophenyl)[2-(methylamino)-5-nitrophenyl]-. Halazepam, hydrolysis. Clorazepate M (hydroxy-), isomer 1, hydrolysis, acetylated.

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