Nalcamine g-13

Physical Properties

Property	Value	Unit	Source
Δ_vapH°	129.20	kJ/mol	Relay (1.0) Calculated Property
logP_oct/wat	5.730		Crippen Calculated Property
McVol	327.210	ml/mol	McGowan Calculated Property
T_fus	309.78	K	Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l 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

Rhodoporphyrin-XV homologue, bis(trimethylsiloxy)silicon(IV) derivative.

4-[2-(4-Allyl-2,6-dimethoxy-phenoxy)-1-hydroxy-propyl]-2-methoxy-phenol, TPS.

3'-Deoxyguanosine, tris(trimethylsilyl) deriv..

Uridine, 2',3'-bis-O-acetyl, 5'-O-TBDMS.

Uridine, 2'-O-TBDMS, 3',5'-bis-O-acetyl.

Uridine, 2'-O-acetyl, 3',5'-bis-O-TBDMS.

(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.

Uridine, 2'-O-TBDMS, 3'-O-acetyl, 5'-O-TBDMS.

Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19«alpha»)-.

Find more compounds similar to Nalcamine g-13.

Sources

Cheméo Relay (1.0)
Cheméo Relay (1.0, beta) Beta: served but experimental, data-limited and below our cross-validation release bar; the Joback value is recommended where available.
Crippen Method
Crippen Method
McGowan Method
NIST Webbook

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.

Chemical Properties of Nalcamine g-13

Physical Properties

Similar Compounds

Sources