Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H28ClNO |
| Molecular Weight | 345.906 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)C(C(=O)C2=CN(CCCCCCl)C3=CC=CC=C23)C1(C)C
InChI
InChIKey=CKIOITGXSRFWIS-UHFFFAOYSA-N
InChI=1S/C21H28ClNO/c1-20(2)19(21(20,3)4)18(24)16-14-23(13-9-5-8-12-22)17-11-7-6-10-15(16)17/h6-7,10-11,14,19H,5,8-9,12-13H2,1-4H3
| Molecular Formula | C21H28ClNO |
| Molecular Weight | 345.906 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
UR-144 N-(5-chloropentyl) analog differs from UR-144 by having a chlorine atom on the terminal carbon of the alkyl group, this compound belongs to the class of synthetic cannabinoid. But this compound is not included in the Schedules to the CDSA (Controlled Drugs and Substances Act) and is not a controlled substance. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity. | 2010 Jan 14 |
|
| UR-144 in products sold via the Internet: identification of related compounds and characterization of pyrolysis products. | 2013 Aug |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:25:24 GMT 2023
by
admin
on
Sat Dec 16 10:25:24 GMT 2023
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| Record UNII |
120SQ2FIK4
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| Record Status |
Validated (UNII)
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120SQ2FIK4
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90464183
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