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
[H][C@@]1(CCCCN1)[C@H](C(=O)OCCC)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
Sat Dec 16 11:23:37 GMT 2023
by
admin
on
Sat Dec 16 11:23:37 GMT 2023
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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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WIKIPEDIA |
Designer-drugs-Propylphenidate
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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| Code System | Code | Type | Description | ||
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PROPYLPHENIDATE
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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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 Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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0Q064445GT
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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PROPYL 2-PHENYL-2-(PIPERIDIN-2-YL)ACETATE
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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PRIMARY | |||
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PROPYLPHENIDATE
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
|
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 Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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DTXSID101032411
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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99088-50-3
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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PPH
Created by
admin on Sat Dec 16 11:23:37 GMT 2023 , Edited by admin on Sat Dec 16 11:23:37 GMT 2023
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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 |
