Prolintane | |
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Salts [] | |
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Prolintane hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C15H23N[1] |
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Molecular mass | 217.35 g/mol[1] |
Predicted LogP | 4[1] |
Boiling point | 153 °C[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(1-phenylpentan-2-yl)pyrrolidine[1] |
SMILES | CCCC(CC1=CC=CC=C1)N2CCCC2[1] |
InChI | InChI=1S/C15H23N/c1-2-8-15(16-11-6-7-12-16)13-14-9-4-3-5-10-14/h3-5,9-10,15H,2,6-8,11-13H2,1H3[1] |
InChIKey | OJCPSBCUMRIPFL-UHFFFAOYSA-N[1] |
Dosing |
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Prolintane
Prolintane (also known as Prolintan, Phenylpyrrolidinopentane, 1-Phenyl-2-pyrrolidinylpentane, Prolintano, Prolintanum, 1-(alpha-Propylphenethyl)pyrrolidine, Pyrrolidine, 1-(1-benzylbutyl)-, Pyrrolidine, 1-(1-(phenylmethyl)butyl)-, 1-(.alpha.-Propylphenethyl)pyrrolidine or Pyrrolidine, 1-(alpha-propylphenethyl)-) is a substance of the amphetamine class.
Chemistry
Prolintane is typically found in the form of its hydrochloride salt.
Stereochemistry
Prolintane is a racemic mixture of the optical stereoisomers