Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C23H30N2O2.ClH |
| Molecular Weight | 402.957 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC(=O)N(C1CCN(CC(O)C2=CC=CC=C2)CC1C)C3=CC=CC=C3
InChI
InChIKey=KQPQDFGRJDIUNS-UHFFFAOYSA-N
InChI=1S/C23H30N2O2.ClH/c1-3-23(27)25(20-12-8-5-9-13-20)21-14-15-24(16-18(21)2)17-22(26)19-10-6-4-7-11-19;/h4-13,18,21-22,26H,3,14-17H2,1-2H3;1H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Studies on potent analgesics. V. Synthesis and analgesic activity of the ester derivatives of N-(1-(2-hydroxy-2-phenylethyl)-3-methyl-4-piperidyl)-N-phenylpropan amide (7302)]. | 1983-11 |
|
| Studies on synthesis and relationship between analgesic activity and receptor affinity for 3-methyl fentanyl derivatives. | 1981-05 |
Patents
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| Code System | Code | Type | Description | ||
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45261717
Created by
admin on Tue Apr 01 16:54:36 GMT 2025 , Edited by admin on Tue Apr 01 16:54:36 GMT 2025
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PRIMARY | |||
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ZJ8A3XT8VW
Created by
admin on Tue Apr 01 16:54:36 GMT 2025 , Edited by admin on Tue Apr 01 16:54:36 GMT 2025
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PRIMARY | |||
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135159-44-3
Created by
admin on Tue Apr 01 16:54:36 GMT 2025 , Edited by admin on Tue Apr 01 16:54:36 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
