Despropionyl-p-fluorofentanyl

Despropionyl-p-fluorofentanyl is an inactive synthetic opioid analgesic drug precursor to 4-fluorofentanyl. It is an analog of fentanyl.

Despropionyl-p-fluorofentanyl

Identifiers
IUPAC name N-phenyl-N-4-piperidinyl-butanamide,
CAS Number	122861-41-0
PubChem CID	21812144
ChemSpider	10551386 N
UNII	R8ZH1EQ95Y
CompTox Dashboard (EPA)	DTXSID10618291
Chemical and physical data
Formula	C19H23FN2O0
Molar mass	298.405 g·mol−1
3D model (JSmol)	Interactive image
SMILES Fc3ccc(NC2CCN(CCc1ccccc1)CC2)cc3
InChI InChI=1S/C19H23FN2/c20-17-6-8-18(9-7-17)21-19-11-14-22(15-12-19)13-10-16-4-2-1-3-5-16/h1-9,19,21H,10-15H2 Key:WWDHLOLWLHHFBH-UHFFFAOYSA-N

See also

• 3-Methylbutyrfentanyl
• 4-Fluorobutyrfentanyl
• 4-Fluorofentanyl
• α-Methylfentanyl
• Acetylfentanyl
• Benzylfentanyl
• Furanylfentanyl
• Homofentanyl
• List of fentanyl analogues

Further reading

• Higashikawa Y, Suzuki S (June 2008). "Studies on 1-(2-phenethyl)-4-(N-propionylanilino)piperidine (fentanyl) and its related compounds. VI. Structure-analgesic activity relationship for fentanyl, methyl-substituted fentanyls and other analogues". Forensic Toxicology. 26 (1): 1–5. doi:10.1007/s11419-007-0039-1. S2CID 22092512.
• Alburges ME, Hanson GR, Gibb JW, Sakashita CO, Rollins DE (1992). "Fentanyl receptor assay. II. Utilization of a radioreceptor assay for the analysis of fentanyl analogs in urine". J Anal Toxicol. 16 (1): 36–41. doi:10.1093/jat/16.1.36. PMID 1322477.
• Woods J, Medzihradsky F, Smith C, Winger G, Gmerek D (1988). "Evaluation of new compounds for opioid activity: 1987 annual report". NIDA Res. Monogr. 81: 543–90. PMID 3136388.
• Aceto M, Bowman E, Harris L, May E (1988). "Dependence studies of new compounds in the rhesus monkey, rat, and mouse, 1987". NIDA Res. Monogr. 81: 485–542. PMID 3136386.
• Brine GA, Boldt KG, Huang PT, Sawyer DK, Carroll FI (2009). "Carbon-13 nuclear magnetic resonance spectra of fentanyl analogs". Journal of Heterocyclic Chemistry. 26 (3): 677–686. doi:10.1002/jhet.5570260329.