Reactions. Piperine forms salts only with strong acids. The platinichloride B4·H2PtCl6 forms orange-red needles ("B" denotes one mole of the alkaloid base in ... Preparation · Reactions |
Chemical structure: C17H19NO3 This structure is also available as a 2d Mol file Stereoisomers: Information on this page: Other data available: |
Piperine is basically an N-acyl pyridine molecule. In other words, the piperine structure depicts that piperidine is substituted by (1E,3E)-1-(1,3-benzodioxol-5 ... |
Piperine ; Molecular formula: C17H19NO3 ; Average mass: 285.343. |
15 авг. 2022 г. · A N-acylpiperidine that is piperidine substituted by a (1E,3E)-1-(1,3-benzodioxol-5-yl)-5-oxopenta-1,3-dien-5-yl group at the nitrogen atom. It ... |
Piperine has a conjugated aliphatic chain that connects the piperidine and 5-(3,4-methylenedioxyphenyl) moiety. This unique structure of piperine may be ... |
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