| Identification | Back Directory | [Name]
7-Methyltryptamine | [CAS]
14490-05-2 | [Synonyms]
NSC 91540
7-METHYLTRYPTAMINE
7-Metyhltryptamine
RARECHEM AN KA 1426
7-Methyltryptamine 98%
7-METHYLTRYPTAMINE free base
7-METHYLTRYPTAMINE CRYSTALLINE
7-methyl-1h-indole-3-ethanamin
3-(2-aminoethyl)-7-methyl-indol
3-(2-AMINOETHYL)-7-METHYLINDOLE
7-methyl-1H-indole-3-ethylamine
1H-Indole-3-ethanaMine, 7-Methyl-
3-(2-Aminoethyl)-7-methyl-1H-indole
2-(7-methyl-1H-indol-3-yl)ethanamine
2-(7-methyl-1H-indol-3-yl)ethanamine hydrochloride
2-(7-methyl-1H-indol-3-yl)ethanamine(SALTDATA: 1.05HCl 0.15H2O) | [EINECS(EC#)]
238-498-9 | [Molecular Formula]
C11H14N2 | [MDL Number]
MFCD00069711 | [MOL File]
14490-05-2.mol | [Molecular Weight]
174.24 |
| Chemical Properties | Back Directory | [Melting point ]
123-130 °C | [Boiling point ]
150-220 °C(Press: 0.03 Torr) | [density ]
1.126±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [form ]
powder | [pka]
17.51±0.30(Predicted) | [InChI]
InChI=1S/C11H14N2/c1-8-3-2-4-10-9(5-6-12)7-13-11(8)10/h2-4,7,13H,5-6,12H2,1H3 | [InChIKey]
SGGBZKQTWMKXHD-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=CC=C2C)C(CCN)=C1 |
| Hazard Information | Back Directory | [Uses]
- Reactant for preparation of β-carbolines via diastereo- and enantioselective Bronsted acid catalyzed N-acyliminium cyclization cascades
- Reactant for preparation of substituted tetrahydro-β-carbolines as potential agents for treatment of human papillomavirus infection (HPV)
- Reactant for asymmetric synthesis of nitrogen heterocycles via Bronsted acid-catalyzed N-acyliminium cyclization cascade
- Reactant for amidation reactions
- Reactant for preparation of potent β3-adrenergic receptor agonists
- Reactant for preparation of tryptamine-based sulfonamides as potent and selective inhibitors of 15-lipoxygenase
| [Uses]
Reactant for preparation of β-carbolines via diastereo- and enantioselective Bronsted acid catalyzed N-acyliminium cyclization cascades 1 Reactant for preparation of substituted tetrahydro-β-carbolines as potential agents for treatment of human papillomavirus infection (HPV) 2 Reactant for asymmetric synthesis of nitrogen heterocycles via Bronsted acid-catalyzed N-acyliminium cyclization cascade 3 Reactant for amidation reactions 4 Reactant for preparation of potent β3-adrenergic receptor agonists 5 Reactant for preparation of tryptamine-based sulfonamides as potent and selective inhibitors of 15-lipoxygenase 6 |
|
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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