CAS 147591-46-6
:1H-Indol-6-ol, 1-(4-methoxyphenyl)-2-methyl-3-nitro-
Description:
1H-Indol-6-ol, 1-(4-methoxyphenyl)-2-methyl-3-nitro- is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This specific compound features a hydroxyl group (-OH) at the 6-position of the indole, a methoxy group (-OCH3) attached to the para position of a phenyl ring, and a nitro group (-NO2) at the 3-position, along with a methyl group (-CH3) at the 2-position. The presence of these functional groups contributes to its potential biological activity and solubility properties. The compound is likely to exhibit various chemical reactivity patterns due to the electron-withdrawing nature of the nitro group and the electron-donating characteristics of the methoxy group. Its molecular structure suggests potential applications in pharmaceuticals or as a precursor in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C16H14N2O4
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Found 10 products.
1-(4-Methoxyphenyl)-2-Methyl-3-Nitro-1H-Indol-6-Ol
CAS:<p>1-(4-Methoxyphenyl)-2-Methyl-3-Nitro-1H-Indol-6-Ol</p>Purity:98%Molecular weight:298.29g/molID 8
CAS:Formula:C16H14N2O4Purity:>98.0%(GC)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:298.30ID-8
CAS:<p>ID-8, a DYRK inhibitor, sustains embryonic stem cell self-renewal in long-term culture.</p>Formula:C16H14N2O4Purity:99.32%Color and Shape:SolidMolecular weight:298.291H-INDOL-6-OL, 1-(4-METHOXYPHENYL)-2-METHYL-3-NITRO-
CAS:Purity:95.0%Molecular weight:298.2980041503906ID 8
CAS:Controlled Product<p>Applications ID 8 is an indole derivative that sustains embryonic stem cell self-renewal in long-term culture.<br>References Miyabayashi, T., et. al.: Biosci. Biotech Bioch., 72, 1242 (2008)<br></p>Formula:C16H14N2O4Color and Shape:NeatMolecular weight:298.293ID 8-d3
CAS:<p>ID 8-d3 is a plant growth stimulant, which is derived from lignin, a complex organic polymer found in the cell walls of many plants and algae. With a deep focus on promoting plant growth and resilience, ID 8-d3 functions through the modulation of key plant physiological processes. Its mode of action involves enhancing nutrient uptake, stimulating root development, and bolstering stress resilience, which is mediated by biochemical pathways that synergize with the plant’s inherent metabolic processes.</p>Formula:C16H11D3N2O4Purity:Min. 95%Molecular weight:301.31 g/mol







