Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H23NO.ClH |
| Molecular Weight | 317.853 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCCC(N1CCCC1)C(=O)C2=CC3=CC=CC=C3C=C2
InChI
InChIKey=SIOVYKZRZLWQSY-UHFFFAOYSA-N
InChI=1S/C19H23NO.ClH/c1-2-7-18(20-12-5-6-13-20)19(21)17-11-10-15-8-3-4-9-16(15)14-17;/h3-4,8-11,14,18H,2,5-7,12-13H2,1H3;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 | C19H23NO |
| Molecular Weight | 281.392 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Sympathomimetic toxicity in a case of analytically confirmed recreational use of naphyrone (naphthylpyrovalerone). | 2011-08 |
|
| The naphyrone story: The alpha or beta-naphthyl isomer? | 2010-10 |
|
| Analyses of second-generation 'legal highs' in the UK: initial findings. | 2010-08 |
|
| 1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors. | 2006-02-23 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:22:27 GMT 2025
by
admin
on
Mon Mar 31 23:22:27 GMT 2025
|
| Record UNII |
4EMP7E490R
|
| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
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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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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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DEA NO. |
1258
Created by
admin on Mon Mar 31 23:22:27 GMT 2025 , Edited by admin on Mon Mar 31 23:22:27 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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53326964
Created by
admin on Mon Mar 31 23:22:27 GMT 2025 , Edited by admin on Mon Mar 31 23:22:27 GMT 2025
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PRIMARY | |||
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850352-11-3
Created by
admin on Mon Mar 31 23:22:27 GMT 2025 , Edited by admin on Mon Mar 31 23:22:27 GMT 2025
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PRIMARY | |||
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4EMP7E490R
Created by
admin on Mon Mar 31 23:22:27 GMT 2025 , Edited by admin on Mon Mar 31 23:22:27 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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