Dimethyl 1H-indole-4,6-dicarboxylate

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Reagent Code: #167325
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CAS Number 86012-83-1

science Other reagents with same CAS 86012-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.22 g/mol
Formula C₁₂H₁₁NO₄
badge Registry Numbers
MDL Number MFCD07781294
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of kinase inhibitors and anti-inflammatory agents. Also employed in the research of fluorescent dyes and optoelectronic materials due to the inherent electron-rich nature of the indole core. The ester groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,670.00
inventory 1g
10-20 days ฿48,950.00

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Dimethyl 1H-indole-4,6-dicarboxylate
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Used in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of kinase inhibitors and anti-inflammatory agents. Also employed in the research of fluorescent dyes and optoelectronic materials due to the inherent electron-rich nature of the indole core. The ester groups allow for easy functionalization, making it valuable in combinatorial che
Used in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of kinase inhibitors and anti-inflammatory agents. Also employed in the research of fluorescent dyes and optoelectronic materials due to the inherent electron-rich nature of the indole core. The ester groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.
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