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CAS 443-31-2

:

3-(2-aminoethyl)-1H-indol-6-ol

Description:
3-(2-aminoethyl)-1H-indol-6-ol, with the CAS number 443-31-2, is an organic compound that features an indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance contains an aminoethyl side chain and a hydroxyl group at the 6-position of the indole ring, contributing to its potential biological activity. The presence of the amino group suggests that it may participate in various chemical reactions, including those involving nucleophilic substitution or hydrogen bonding. The hydroxyl group can also engage in hydrogen bonding, influencing the compound's solubility and reactivity. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarity to various biologically active molecules. Additionally, its characteristics may include moderate polarity, which can affect its interaction with biological systems and its overall pharmacokinetic profile. Further studies would be necessary to fully elucidate its biological properties and potential applications.
Formula:C10H12N2O
InChI:InChI=1/C10H12N2O/c11-4-3-7-6-12-10-5-8(13)1-2-9(7)10/h1-2,5-6,12-13H,3-4,11H2
SMILES:c1cc2c(CCN)c[nH]c2cc1O
Synonyms:
  • 6-Hydroxytryptamine
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Found 2 products.
  • 3-(2-aminoethyl)-1H-indol-6-ol
    Indagoo
    + Info

    3-(2-aminoethyl)-1H-indol-6-ol

    CAS:
    Formula:C10H12N2O
    Purity:95%
    Molecular weight:176.2151

    Ref: IN-DA00DLXH

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  • 3-(2-Aminoethyl)-1H-indol-6-ol
    Biosynth
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    3-(2-Aminoethyl)-1H-indol-6-ol

    Controlled Product
    CAS:
    <p>3-(2-Aminoethyl)-1H-indol-6-ol (3-OH-6) is a compound that is structurally related to the neurotransmitter acetylcholine. It has been shown to have an inhibitory effect on amines and blood pressure in cell culture. 3-OH-6 also has the ability to bind to model proteins such as tyrosinase. This binding inhibits the uptake of 3-OH-6, which leads to its accumulation in cells where it can cause damage by acting on adrenergic receptors. 3-(2 Aminoethyl)-1H-indol-6-ol’s ability to act on dopamine receptors may be due to its hydroxyl group.</p>
    Formula:C10H12N2O
    Purity:Min. 95%
    Molecular weight:176.21 g/mol

    Ref: 3D-AAA44331

    50mg
    624.00€
    500mg
    1,746.00€