Chemical Properties of Maprotiline M(di-HO), diacetylated

Maprotiline M(di-HO), diacetylated

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InChI
InChI=1S/C24H27NO4/c1-15(26)25(3)12-4-10-24-11-9-19(20-7-5-17(28)13-22(20)24)21-8-6-18(14-23(21)24)29-16(2)27/h5-8,13-14,19,28H,4,9-12H2,1-3H3
InChI Key
DFNVBHIKRFICNK-UHFFFAOYSA-N
Formula
C24H27NO4
SMILES
CC(=O)Oc1ccc2c(c1)C1(CCCN(C)C(C)=O)CCC2c2ccc(O)cc21
Molecular Weight1
393.48
Sources

Physical Properties

Property Value Unit Source
Δf 80.66 kJ/mol Joback Calculated Property
Δfgas -394.04 kJ/mol Joback Calculated Property
Δfus 52.19 kJ/mol Joback Calculated Property
Δvap 104.85 kJ/mol Joback Calculated Property
logPoct/wat 4.10 Crippen Calculated Property
Pc 1744.82 kPa Joback Calculated Property
Tboil 1045.22 K Joback Calculated Property
Tc 1289.34 K Joback Calculated Property
Tfus 783.74 K Joback Calculated Property
Vc 1.11 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1058.24 J/mol×K 1045.22 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>C=O (nonring) 2
=CH- (ring) 6
>N- 1
=C< (ring) 6
-CH2- 3
>C< (ring) 1
-CH3 3
>CH- (ring) 1
-OH (phenol) 1
-CH2- (ring) 2

Similar Compounds

Maprotiline M(Nor-HO), diacetylated. Maprotiline M(tri-HO), triacetylated. Melitracene M(Nor-HO-dihydro), diacetylated. Maprotiline, N-acetyl-. Maprotiline M(Nor), acetyl conjugate. Maprotiline. Protriptyline M(HO), acetylated. Maprotiline M(HO-ethanediyl), diacetylated. Maprotiline M(HO-propyl), acetylated. (6R,7S,8S)-8-(4-Hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol. Maprotiline M(HO-anthryl), diacetylated. Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one, 5,8,8a,9-tetrahydro-5-(3,4,5-trimethoxyphenyl)-, [5R-(5«alpha»,5a«beta»,8a«alpha»)]-. 9,10-Ethanoanthracene-9(10h)-methylamine, n-methyl-, 9,10-dihydro. Nalmefene, trimethylsilyl ether. (7R,8S)-8-(4-Hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-7,8-dihydronaphthalen-2-ol.

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