Methyl 3-formyl-1-methyl-1H-indole-2-carboxylate

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Reagent Code: #205700
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CAS Number 88129-40-2

science Other reagents with same CAS 88129-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD07364648
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of indole-based drugs. Its structure supports the construction of complex heterocyclic systems found in medicinal chemistry. Commonly employed in research settings for creating analogs with potential anti-inflammatory, anticancer, or neurological activity. Also utilized in agrochemical research for designing new active ingredients. Its aldehyde and ester functional groups allow for diverse chemical modifications, making it valuable in combinatorial chemistry and drug discovery.

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inventory 100mg
10-20 days ฿17,920.00

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Methyl 3-formyl-1-methyl-1H-indole-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of indole-based drugs. Its structure supports the construction of complex heterocyclic systems found in medicinal chemistry. Commonly employed in research settings for creating analogs with potential anti-inflammatory, anticancer, or neurological activity. Also utilized in agrochemical research for designing new active ingredients. Its aldehyde and ester functional groups allow f

Used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of indole-based drugs. Its structure supports the construction of complex heterocyclic systems found in medicinal chemistry. Commonly employed in research settings for creating analogs with potential anti-inflammatory, anticancer, or neurological activity. Also utilized in agrochemical research for designing new active ingredients. Its aldehyde and ester functional groups allow for diverse chemical modifications, making it valuable in combinatorial chemistry and drug discovery.

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