Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H16FN3O2 |
| Molecular Weight | 397.4011 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=C(CN2N=C(C(=O)OC3=C4N=CC=CC4=CC=C3)C5=C2C=CC=C5)C=C1
InChI
InChIKey=NYHGKZZRRCVGAU-UHFFFAOYSA-N
InChI=1S/C24H16FN3O2/c25-18-12-10-16(11-13-18)15-28-20-8-2-1-7-19(20)23(27-28)24(29)30-21-9-3-5-17-6-4-14-26-22(17)21/h1-14H,15H2
| Molecular Formula | C24H16FN3O2 |
| Molecular Weight | 397.4011 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 18:16:55 UTC 2023
by
admin
on
Sat Dec 16 18:16:55 UTC 2023
|
| Record UNII |
2DC7C24RQX
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
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| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-FUB-NPB-22
Created by
admin on Sat Dec 16 18:16:55 UTC 2023 , Edited by admin on Sat Dec 16 18:16:55 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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2DC7C24RQX
Created by
admin on Sat Dec 16 18:16:55 UTC 2023 , Edited by admin on Sat Dec 16 18:16:55 UTC 2023
|
PRIMARY | |||
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2244864-90-0
Created by
admin on Sat Dec 16 18:16:55 UTC 2023 , Edited by admin on Sat Dec 16 18:16:55 UTC 2023
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PRIMARY | |||
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125181354
Created by
admin on Sat Dec 16 18:16:55 UTC 2023 , Edited by admin on Sat Dec 16 18:16:55 UTC 2023
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PRIMARY | |||
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16883
Created by
admin on Sat Dec 16 18:16:55 UTC 2023 , Edited by admin on Sat Dec 16 18:16:55 UTC 2023
|
PRIMARY | PB-22 (Item No. 14096), first reported in 2013, introduced 8-hydroxyquinoline as a substitution for the naphthalene group on traditional JWH-type synthetic cannabinoids. The analog NPB-22 (Item No. 15535) differs from PB-22 by the replacement of indazole for indole. FUB-NPB-22 is an analog of NPB-22 in which the pentyl side chain is replaced by a 4-fluorobenzyl group. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications. |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
