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1199943-44-6

1199943-44-6 Structure

1199943-44-6 Structure
IdentificationBack Directory
[Name]

(1-pentyl-1H-indol-3-yl) (2, 2, 3, 3-tetraMethyl-cyclopropyl) Methanone
[CAS]

1199943-44-6
[Synonyms]

KM-X1
YX-17
MN-001
UR-144
CS-172
TMCP-018
UR-144 (CRM)
UR-144 solution
(1-Pentyl-1H-indol-3-yl)(2,2,3,3-tetraMethylcycl
(1-pentylindol-3-yl)-(2,2,3,3-tetraMethylcyclopropyl)Methanone
Methanone, (1-pentyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)-
(1-pentyl-1H-indol-3-yl) (2, 2, 3, 3-tetraMethyl-cyclopropyl) Methanone
(1-Pentyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone (UR-144)
UR-144((1-pentyl-1H-indol-3-yl) (2, 2, 3, 3-tetraMethyl-cyclopropyl) Methanone)
(1-Pentyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone (UR-144) (1.0 mg/mL in Methanol)
[EINECS(EC#)]

200-659-6
[Molecular Formula]

C21H29NO
[MDL Number]

MFCD21340157
[MOL File]

1199943-44-6.mol
[Molecular Weight]

311.46
Chemical PropertiesBack Directory
[Boiling point ]

426.6±18.0 °C(Predicted)
[density ]

1.03
[storage temp. ]

-20°C
[solubility ]

DMF: 30 mg/ml
DMSO: 30 mg/ml
Ethanol: 30 mg/ml
[form ]

A neat solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P321-P330-P362+P364-P501
[Hazard Codes ]

F,T
[Risk Statements ]

11-23/24/25-39/23/24/25
[Safety Statements ]

7-16-36/37-45
Hazard InformationBack Directory
[Description]

UR-144 (Item No. ISO00055) is an analytical reference material categorized as a synthetic cannabinoid. It has been found in Spice/K2-type herbal blends. UR-144 is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications.
[Uses]

(1-Pentyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone is an Indol-3-ylcycloalkyl Ketone with high affinity for the CB2 cannabinoid receptor. Tetramethylcyclopropyl group was found to lead to high affinity CB2 agonists. Synthetic Cannabinoids
[References]

[1] JENNIFER M. FROST*. Indol-3-ylcycloalkyl Ketones: Effects of N1 Substituted Indole Side Chain Variations on CB2 Cannabinoid Receptor Activity[J]. Journal of Medicinal Chemistry, 2009, 53 1: 295-315. DOI: 10.1021/jm901214q
[2] KATHRYN A. SEELY . Forensic investigation of K2, Spice, and “bath salt” commercial preparations: A three-year study of new designer drug products containing synthetic cannabinoid, stimulant, and hallucinogenic compounds[J]. Forensic science international, 2013, 233 1: Pages 416-422. DOI: 10.1016/j.forsciint.2013.10.002
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