Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H29FN2O |
| Molecular Weight | 368.4876 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(=O)N(C1CCN(CCC2=CC=CC=C2)CC1)C3=CC=C(F)C=C3
InChI
InChIKey=QZFMCYUBPSLOBP-UHFFFAOYSA-N
InChI=1S/C23H29FN2O/c1-2-6-23(27)26(21-11-9-20(24)10-12-21)22-14-17-25(18-15-22)16-13-19-7-4-3-5-8-19/h3-5,7-12,22H,2,6,13-18H2,1H3
Approval Year
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-4-Fluorobutyrfentanyl
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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DEA NO. |
9823
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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4-FLUOROBUTYRFENTANYL
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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SUB180990
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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100000166746
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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244195-31-1
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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86280430
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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4-FLUOROBUTYRFENTANYL
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear. | ||
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DTXSID101032566
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY | |||
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2378L0E82T
Created by
admin on Mon Mar 31 23:20:51 GMT 2025 , Edited by admin on Mon Mar 31 23:20:51 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)