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Substituted phenidates: Difference between revisions

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>Dextromethorphan
>BronzeManul
List of substituted phenidates: Added 4-Methyl Methylphenidate
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| [[Propylphenidate]] || H || H || CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:Propylphenidate.png|170px]]
| [[Propylphenidate]] || H || H || CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:Propylphenidate.png|170px]]
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| [[4-Methyl Methylphenidate]] || H || CH<sub>3</sub> || CH<sub>3</sub> || [[File:4Me-MPH.png|171px]]
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| [[3,4-CTMP]] || Cl || Cl || CH<sub>3</sub> || [[File:34-ctmp.png|171px]]
| [[3,4-CTMP]] || Cl || Cl || CH<sub>3</sub> || [[File:34-ctmp.png|171px]]

Revision as of 00:02, 26 October 2016

General formula of a phenidate molecule.

Substituted phenidates, also known as phenidates, are a class of chemicals that include compounds with psychoactive effects.

Chemistry

Substituted phenidates are a chemical class based upon the molecule Methylphenidate. Methylphenidate is made up of a phenethylamine molecule with a carbon chain substitution at the Rα position that links to the RN position forming a piperidine ring, and a substitution at the Rβ position of methyl acetate.

List of substituted phenidates

Compound R3 R4 RO Structure
Methylphenidate H H CH3
Ethylphenidate H H CH2CH3
Isopropylphenidate H H CH(CH3)2
Propylphenidate H H CH2CH2CH3
4-Methyl Methylphenidate H CH3 CH3
3,4-CTMP Cl Cl CH3
4F-MPH H F CH3
4F-EPH H F CH2CH3
Methylnaphthidate CH=CH- CH=CH- CH3
Ethylnaphthidate CH=CH- CH=CH- CH2CH3

See also