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Substituted phenidates: Difference between revisions

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|-
|-
! scope="col" | '''Compound'''
! scope="col" | '''Compound'''
! scope="col" style="width: 50px;" | '''R<sub>2</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>3</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>3</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>4</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>4</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>5</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>6</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>O</sub>'''
! scope="col" style="width: 50px;" | '''R<sub>O</sub>'''
! scope="col" | '''Structure'''
! scope="col" | '''Structure'''
|-
|-
| [[Methylphenidate]] || H || H || H || H || H || CH<sub>3</sub> || [[File:Methyllphenidate.png|170px]]
| [[Methylphenidate]] || H || H || CH<sub>3</sub> || [[File:Methyllphenidate.png|170px]]
|-
|-
| [[Ethylphenidate]] || H || H || H || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethyllphenidate.png|170px]]
| [[Ethylphenidate]] || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethyllphenidate.png|170px]]
|-
|-
| [[Isopropylphenidate]] || H || H || H || H || H || CH(CH<sub>3</sub>)<sub>2</sub> || [[File:Isopropylphenidate.png|170px]]
| [[Isopropylphenidate]] || H || H || CH(CH<sub>3</sub>)<sub>2</sub> || [[File:Isopropylphenidate.png|170px]]
|-
|-
| [[Propylphenidate]] || H || H || H || 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]]
|-
|-
| [[3,4-CTMP]] || H || Cl || Cl || H || H || CH<sub>3</sub> || [[File:34-ctmp.png|170px]]
| [[3,4-CTMP]] || Cl || Cl || CH<sub>3</sub> || [[File:34-ctmp.png|170px]]
|-
|-
| [[4F-MPH]] || H || H || F || H || H || CH<sub>3</sub> || [[File:4-Fluoromethylphenidate.png|170px]]
| [[4F-MPH]] || H || F || CH<sub>3</sub> || [[File:4-Fluoromethylphenidate.png|170px]]
|-
|-
| [[4F-EPH]] || H || H || F || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:4F-EPH.png|170px]]
| [[4F-EPH]] || H || F || CH<sub>2</sub>CH<sub>3</sub> || [[File:4F-EPH.png|170px]]
|-
|-
| [[Methylnaphthidate]] || H || CH=CH- || CH=CH- || H || H || CH<sub>3</sub> || [[File:Methylnaphthidate.png|170px]]
| [[Methylnaphthidate]] || CH=CH- || CH=CH- || CH<sub>3</sub> || [[File:Methylnaphthidate.png|170px]]
|-
|-
| [[Ethylnaphthidate]] || H || CH=CH- || CH=CH- || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethylnaphthidate.png|170px]]
| [[Ethylnaphthidate]] || CH=CH- || CH=CH- || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethylnaphthidate.png|170px]]
|-
|-
|}
|}

Revision as of 20:08, 25 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
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

Retrieved from "http://psy.st/w/index.php?title=Substituted_phenidates&oldid=71303"