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
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C23H30N2O2 |
| Molecular Weight | 366.4965 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Studies on synthesis and relationship between analgesic activity and receptor affinity for 3-methyl fentanyl derivatives. | 1981 May |
|
| [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 Nov |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:45:09 GMT 2023
by
admin
on
Sat Dec 16 11:45:09 GMT 2023
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| Record UNII |
ZJ8A3XT8VW
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| Record Status |
Validated (UNII)
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| Record Version |
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45261717
Created by
admin on Sat Dec 16 11:45:09 GMT 2023 , Edited by admin on Sat Dec 16 11:45:09 GMT 2023
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ZJ8A3XT8VW
Created by
admin on Sat Dec 16 11:45:09 GMT 2023 , Edited by admin on Sat Dec 16 11:45:09 GMT 2023
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135159-44-3
Created by
admin on Sat Dec 16 11:45:09 GMT 2023 , Edited by admin on Sat Dec 16 11:45:09 GMT 2023
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PRIMARY |
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PARENT -> SALT/SOLVATE |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
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ACTIVE MOIETY |
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