Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H17Cl2NO2 |
| Molecular Weight | 302.196 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]([C@H]1CCCCN1)C2=CC=C(Cl)C(Cl)=C2
InChI
InChIKey=JUKMAYKVHWKRKY-CHWSQXEVSA-N
InChI=1S/C14H17Cl2NO2/c1-19-14(18)13(12-4-2-3-7-17-12)9-5-6-10(15)11(16)8-9/h5-6,8,12-13,17H,2-4,7H2,1H3/t12-,13-/m1/s1
Approval Year
| Name | Type | Language | ||
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Preferred Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-3,4-Dichloromethylphenidate
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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3,4-DICHLOROMETHYLPHENIDATE
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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PRIMARY | 3,4-CTMP, the threo-diastereomer, is approximately seven times more potent than methylphenidate in animal studies, but has weaker reinforcing effects due to its slower onset of action. However, H. M. Deutsch's discrimination ratio implies it to be more reinforcing than cocaine. | ||
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DTXSID301029379
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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3,4-DICHLOROMETHYLPHENIDATE
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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PRIMARY | 3,4-CTMP is also known as 3,4-dichloro-transmethylphenidate or less frequently as methyl (2R)-2-(3,4-dichlorophenyl)-2-[(2R)-piperidin-2-yl]acetate. 3,4 CTMP is a derivative of methylphenidate which itself is more commonly known as its brand name Ritalin which is used to treat ADD & ADHD. | ||
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1364331-88-3
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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1MM9174NWD
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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44296390
Created by
admin on Mon Mar 31 23:18:43 GMT 2025 , Edited by admin on Mon Mar 31 23:18:43 GMT 2025
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ACTIVE MOIETY
