3-Methylmethcathinone
Compound with spectra: 1 NMR, 1 FTIR, and 7 MS (GC)
| SpectraBase Compound ID | JkwBrS8bYCo |
|---|---|
| InChI | InChI=1S/C11H15NO/c1-8-5-4-6-10(7-8)11(13)9(2)12-3/h4-7,9,12H,1-3H3 |
| InChIKey | QDNXSIYWHYGMCD-UHFFFAOYSA-N |
| Mol Weight | 177.25 g/mol |
| Molecular Formula | C11H15NO |
| Exact Mass | 177.115364 g/mol |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Buy Research Chem., Nerja, Spain |
| Source of Spectrum | Forensic Spectral Research |
| Technique | Film (Dichloromethane) |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | SWG-33-3772-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | John D. Power, et al. Forensic Science International, V.212, 2011, P.6-12 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Niamh Nic Daeid, et al. Science and Justice, 10.1016/j.scijus.2013.08.004 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3_OR_DMSO-D6 |
- 3MMC
- The HCl salt was dissolved in 0.5 ml water in a test tube, and 1 drop of 30% NaOH solution was added, causing the clear solution to turn cloudy white. 1 ml dichloromethane was added to the test tube, which was shaken thoroughly using a vortex mixer. The test tube was spun in a centrifuge to separate the organic and aqueous layers. The bottom organic layer was retrieved with a pipette and placed in another clean test tube. Most of the solvent was evaporated from the tube using a flow of nitrogen gas, and the remaining solution was used to create a film on a KBr wafer for Transmission IR.
- 3-METHYLMETHCATHINONE;2-(METHYLAMINO)-1-(3-METHYLPHENYL)-PROPAN-1-ONE;3-MMC
- 2-(methylamino)-1-(m-tolyl)propan-1-one
- 1-(3-Methylphenyl)-2-methylaminopropan-1-one
1-(3,5-difluorophenyl)-2-(methylamino)propan-1-one
3,5-DIFLUOROMETHCATHINONE-HYDROCHLORIDE
3,5-DICHLOROMETHCATHINONE-HYDROCHLORIDE
1-(3,5-dichlorophenyl)-2-(methylamino)propan-1-one
1-Phenyl-2-benzylaminopropan-1-one
3-Phenyl-1-(3-tolyl)-propan-1-one
2-(N-Anilino)propiophenone
N-(B-[3-Toluoyl]-ethyl)-B-alanine ethyl ester
N-(B-[3-Toluoyl]-ethyl)-B-alanine ethyl ester cation
N-(Ethoxycarbonyl)cathinone
| Title | Journal or Book | Year |
|---|---|---|
| 10.1016/j.forsciint.2011.04.020>10.1016/j.forsciint.2011.04.020 | "" | "" |
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