CAS 77872-43-6
:3-[2-[Methyl(1-methylethyl)amino]ethyl]-1H-indol-4-ol
Description:
3-[2-[Methyl(1-methylethyl)amino]ethyl]-1H-indol-4-ol, with the CAS number 77872-43-6, is a chemical compound that belongs to the indole family, characterized by its indole core structure which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound features a hydroxyl group (-OH) at the 4-position of the indole ring, which can influence its solubility and reactivity. The presence of a methyl(1-methylethyl)amino group at the 2-position contributes to its potential biological activity, as amines can participate in various interactions with biological targets. The compound's structure suggests it may exhibit properties relevant to medicinal chemistry, possibly acting as a ligand or modulator in biological systems. Its specific characteristics, such as solubility, stability, and reactivity, would depend on environmental conditions and the presence of other chemical species. Further studies would be necessary to elucidate its full range of properties and potential applications.
Formula:C14H20N2O
InChI:InChI=1S/C14H20N2O/c1-10(2)16(3)8-7-11-9-15-12-5-4-6-13(17)14(11)12/h4-6,9-10,15,17H,7-8H2,1-3H3
InChI key:InChIKey=RXKGHZCQFXXWFQ-UHFFFAOYSA-N
SMILES:C(CN(C(C)C)C)C=1C=2C(NC1)=CC=CC2O
Synonyms:- Miprocin
- 3-[2-[Methyl(1-methylethyl)amino]ethyl]-1H-indol-4-ol
- 1H-Indol-4-ol, 3-[2-[methyl(1-methylethyl)amino]ethyl]-
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Found 2 products.
4-Hydroxy-N-isopropyl-N-methyltryptamine
CAS:Controlled Product<p>Applications A related homologue of Psilocin.<br>References de Boer, D., et al.: Pharm. World Sci., 26, 110 (2004), Brandt, S., et al.: Analyst, 130, 330 (2005), Matsumoto, T., et al.: J. Health Sci., 52, 805 (2006),<br></p>Formula:C14H20N2OColor and Shape:NeatMolecular weight:232.324-Hydroxy-N-isopropyl-N-methyltryptamine
CAS:Controlled Product4-Hydroxy-N-isopropyl-N-methyltryptamine (4OHMIT) is an analytical chemical that has been shown to bind to various receptors in the rat brain. 4OHMIT has also been found to inhibit the binding of serotonin, dopamine and norepinephrine. This drug is a synthetic compound that has been detected in human urine samples.br>br>4OHMIT is a psychedelic substance that can be used for the acute treatment of depressive disorders and anxiety. It also has pharmacological treatments, such as analytical chemistry, which can be used to detect this drug in biological samples.Formula:C14H20N2OPurity:Min. 95%Molecular weight:232.32 g/mol

