Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCOC(=O)[C@@H]([C@H]1CCCCN1)C2=CC=CC=C2
InChI
InChIKey=PRMWWEANNQSWAR-HUUCEWRRSA-N
InChI=1S/C16H23NO2/c1-2-12-19-16(18)15(13-8-4-3-5-9-13)14-10-6-7-11-17-14/h3-5,8-9,14-15,17H,2,6-7,10-12H2,1H3/t14-,15-/m1/s1
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:23:44 GMT 2025
by
admin
on
Tue Apr 01 16:23:44 GMT 2025
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| Record UNII |
0Q064445GT
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| Record Status |
Validated (UNII)
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| Record Version |
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-Propylphenidate
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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PROPYLPHENIDATE
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | Propylphenidate (also known as PPH) is a piperidine based stimulant drug, closely related to methylphenidate, but with the methyl ester replaced by an propyl ester. It was banned in the UK as a Temporary Class Drug from April 2015 following its unapproved sale as a designer drug. Propylphenidate can be synthesised from methylphenidate. | ||
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119025958
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | |||
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DTXSID801344980
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | |||
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0Q064445GT
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | |||
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PROPYL 2-PHENYL-2-(PIPERIDIN-2-YL)ACETATE
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | |||
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PROPYLPHENIDATE
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
|
PRIMARY | Propylphenidate (also known as PPH) is a piperidine based stimulant drug, closely related to methylphenidate, but with the methyl ester replaced by an propyl ester. It was banned in the UK as a Temporary Class Drug from April 2015 following its unapproved sale as a designer drug.[1] Propylphenidate can be synthesised from methylphenidate.[2] Legal status: Propylphenidate is illegal in Sweden as of 26. January 2016.[3] See also: ?3,4-Dichloromethylphenidate ?4-Fluoromethylphenidate ?4-Methylmethylphenidate?Dexmethylphenidate ?Ethylphenidate ?Isopropylphenidate ?HDEP-28 ?HDMP-28References 1. Methylphenidate-based NPS: A review of the evidence of use and harm. Advisory Council on the Misuse of Drugs, 31 March 2015 2. James Alain Bourland (1997). "The influence of ethanol on drug metabolism and disposition via carboxylesterase-mediated transesterification". 3. "31 nya ?mnen kan klassas som narkotika eller h?lsofarlig vara" (in Swedish). Folkh?lsomyndigheten. November 2015. | ||
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1071564-47-0
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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NON-SPECIFIC STEREOCHEMISTRY | |||
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99088-50-3
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY | |||
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PPH
Created by
admin on Tue Apr 01 16:23:45 GMT 2025 , Edited by admin on Tue Apr 01 16:23:45 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
