Chemical Properties of Nifedipine M (dehydro-bis-carboxy, methyl ester)

Nifedipine M (dehydro-bis-carboxy, methyl ester)

InChI
InChI=1S/C18H16N2O8/c1-9-12(16(21)26-2)13(10-7-5-6-8-11(10)20(24)25)14(17(22)27-3)15(19-9)18(23)28-4/h5-8H,1-4H3
InChI Key
RVORVWKPTSHPSE-UHFFFAOYSA-N
Formula
C18H16N2O8
SMILES
COC(=O)c1nc(C)c(C(=O)OC)c(-c2ccccc2[N+](=O)[O-])c1C(=O)OC
Molecular Weight1
388.33
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Physical Properties

Property Value Unit Source
log10WS -3.79 Relay (1.0) Calculated Property
logPoct/wat 2.325 Crippen Calculated Property
McVol 266.680 ml/mol McGowan Calculated Property
Inp [2695.00; 2695.00]   Show Hide
Inp 2695.00 NIST
Inp 2695.00 NIST
Tboil 676.41 K Relay (1.0) Calculated Property
Tfus 406.83 K Relay (1.0) Calculated Property

Cheméo can also estimate Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy 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

Nifedipine M (dehydro). Nimodipine M (dehydro-desmethoxyethyl, methyl ester). Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19«alpha»)-. (1'S,3R,4a'S,5a'S,10a'S)-Methyl 1'-methyl-2-oxo-1',4a',5',5a',7',8',10',10a'-octahydrospiro[indoline-3,6'-pyrano[3,4-f]indolizine]-4'-carboxylate. Cialis. xanthosine, TMS. Cilostazol. Nitrendipine M (dehydro-desethyl, methyl ester). Hydromorphone, tert-butyldimethylsilyl ether. Thymidine, 3'-O-acetyl, 5'-O-cyclotetramethylene-tertbutylsilyl. CODEIN-PROPIONYL. PACLITAXEL. Triazolo[4,5-d]pyrimidin-7-ol,3h-v-, 5-amino-3-(2',3'-o-isopropylidene-beta-d-ribofuranosyl)-, 5'-diphenyl phosphate (keto form). [2,2'-Bimorphinan]-3,3',6,6'-tetrol, 7,7',8,8'-tetradehydro-4,5:4',5'-diepoxy-17,17'-dimethyl-, (5«alpha»,6«alpha»)-(5'«alpha»,6'«alpha»)-. Ergocristine.

Find more compounds similar to Nifedipine M (dehydro-bis-carboxy, methyl ester).

Sources

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