Chemical Properties of Melitracene M(Nor-HO-dihydro), diacetylated

Melitracene M(Nor-HO-dihydro), diacetylated

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InChI
InChI=1S/C24H29NO3/c1-16(26)25(5)14-8-10-19-20-9-6-7-11-22(20)24(3,4)23-15-18(28-17(2)27)12-13-21(19)23/h6-7,9,11-13,15,19H,8,10,14H2,1-5H3
InChI Key
SVWVOZFNOCWJEJ-UHFFFAOYSA-N
Formula
C24H29NO3
SMILES
CC(=O)Oc1ccc2c(c1)C(C)(C)c1ccccc1C2CCCN(C)C(C)=O
Molecular Weight1
379.49
Sources

Physical Properties

Property Value Unit Source
Δf 154.72 kJ/mol Joback Calculated Property
Δfgas -316.03 kJ/mol Joback Calculated Property
Δfus 47.25 kJ/mol Joback Calculated Property
Δvap 91.78 kJ/mol Joback Calculated Property
logPoct/wat 4.64 Crippen Calculated Property
Pc 1391.25 kPa Joback Calculated Property
Tboil 957.46 K Joback Calculated Property
Tc 1186.82 K Joback Calculated Property
Tfus 646.32 K Joback Calculated Property
Vc 1.17 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1015.72 J/mol×K 957.46 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>C=O (nonring) 2
=CH- (ring) 7
>N- 1
=C< (ring) 5
-CH2- 3
>C< (ring) 1
-CH3 5
>CH- (ring) 1

Similar Compounds

Maprotiline M(di-HO), diacetylated. Maprotiline M(Nor-HO), diacetylated. Maprotiline M(tri-HO), triacetylated. Protriptyline M(HO), acetylated. (6R,7S,8S)-8-(4-Hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol. Maprotiline, N-acetyl-. Maprotiline M(Nor), acetyl conjugate. Maprotiline. Maprotiline M(HO-ethanediyl), diacetylated. (7R,8S)-8-(4-Hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-7,8-dihydronaphthalen-2-ol. 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. Maprotiline M(HO-propyl), acetylated. Maprotiline M(HO-anthryl), diacetylated. Chlorprothixene M (HO-dihydro-), monoacetylated.

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