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| (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone Basic information |
| Product Name: | (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone | | Synonyms: | (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone;tert-butyl 4-acetoxy-octahydroindole-1-carboxylate;Methanone, 1H-indol-3-yl(2,2,3,3-tetramethylcyclopropyl)-;UR-144 Impurity 3 | | CAS: | 895152-66-6 | | MF: | C16H19NO | | MW: | 241.33 | | EINECS: | | Product Categories: | | Mol File: | 895152-66-6.mol |
| (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone Chemical Properties |
| Boiling point | 375.0±15.0 °C(Predicted) | | density | 1.099±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 15.50±0.30(Predicted) | | InChI | InChI=1S/C16H19NO/c1-15(2)14(16(15,3)4)13(18)11-9-17-12-8-6-5-7-10(11)12/h5-9,14,17H,1-4H3 | | InChIKey | WYZQBEQQQKCTHM-UHFFFAOYSA-N | | SMILES | C(C1C2=C(NC=1)C=CC=C2)(C1C(C)(C)C1(C)C)=O |
| (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone Usage And Synthesis |
| Description | UR-144 and XLR11 are potent synthetic cannabinoids (CBs) that have been identified as adulterants of herbal products. (1H-Indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone is the scaffold for UR-144, XLR11, and a number of additional synthetic CBs. The tetramethylcyclopropyl group typically confers selectivity for the peripheral CB2 receptor. However, the addition of substituents at the N1-amine of the aminoalkylindole group is necessary for high affinity at either CB1 or CB2. This product is intended for forensic and research applications. | | Uses | (1H-Indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone is the scaffold for UR-144, XLR11, and a number of additional synthetic CBs. The tetramethylcyclopropyl group typically confers selectivity for the peripheral CB2 receptor |
| (1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone Preparation Products And Raw materials |
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