Methyl 3-formyl-1H-indole-7-carboxylate

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Reagent Code: #208697
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CAS Number 312973-24-3

science Other reagents with same CAS 312973-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
badge Registry Numbers
MDL Number MFCD00550641
thermostat Physical Properties
Boiling Point 404.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of fluorescent dyes and sensors due to the aldehyde and ester functional groups enabling conjugation and derivatization. Also utilized in research for developing potential kinase inhibitors and anti-inflammatory agents. Serves as a building block in the synthesis of tryptamine-related analogs for neurological studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,530.00
inventory 250mg
10-20 days ฿2,990.00
inventory 1g
10-20 days ฿7,450.00

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Methyl 3-formyl-1H-indole-7-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of fluorescent dyes and sensors due to the aldehyde and ester functional groups enabling conjugation and derivatization. Also utilized in research for developing potential kinase inhibitors and anti-inflammatory agents. Serves as a building block in the synthesis of trypta

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry. Commonly employed in the preparation of fluorescent dyes and sensors due to the aldehyde and ester functional groups enabling conjugation and derivatization. Also utilized in research for developing potential kinase inhibitors and anti-inflammatory agents. Serves as a building block in the synthesis of tryptamine-related analogs for neurological studies.

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