Triprolidine | |
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Salts [] | |
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Triprolidine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C19H22N2[1] |
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Molecular mass | 278.4 g/mol[1] |
Appearance | Crystals from light petroleum[1] |
Predicted LogP | 3.9[1] |
Melting point | 59-61 °C[1] |
Solubility | 5.37e-02 g/L[1] |
Chirality | achiral[2] |
Identifiers [] | |
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IUPAC name | 2-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-enyl]pyridine[1] |
SMILES | CC1=CC=C(C=C1)/C(=C\CN2CCCC2)/C3=CC=CC=N3[1] |
InChI | InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+[1] |
InChIKey | CBEQULMOCCWAQT-WOJGMQOQSA-N[1] |
Dosing |
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Triprolidine
Triprolidine (also known as Triprolidin, Tripolidina, Triprolidinum, Triprolidina, CCRIS 7212, trans-1-(2-Pyridyl)-3-pyrrolidino-1-p-tolylprop-1-ene, NCI-C61450, trans-1-(4-Methylphenyl)-1-(2-pyridyl)-3-pyrrolidinoprop-1-ene, trans-2-(3-(1-Pyrrolidinyl)-1-p-tolylpropenyl)pyridine or (E)-2-(1-(4-Methylphenyl)-3-(1-pyrrolidinyl)-1-propenyl)pyridine) is a substance of the phenidate class.
Chemistry
Triprolidine is typically found in the form of its hydrochloride salt.
Stereochemistry
Triprolidine is a achiral mixture