1-Methyl-1H-indole-3-carbonyl chloride

95%

Reagent Code: #202964
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CAS Number 126921-19-5

science Other reagents with same CAS 126921-19-5

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scatter_plot Molecular Information
Weight 193.63 g/mol
Formula C₁₀H₈ClNO
badge Registry Numbers
MDL Number MFCD13174236
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines to form indole-based amides, which are key structural motifs in bioactive molecules. Commonly employed in the development of serotonin receptor ligands and other neuroactive compounds due to the indole core’s prevalence in neurotransmitters. Also utilized in the preparation of fluorescent probes and dyes, where the indole scaffold contributes to light absorption and emission properties. Its reactivity allows for efficient derivatization in combinatorial chemistry and drug discovery pipelines.

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inventory 250mg
10-20 days ฿2,980.00

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1-Methyl-1H-indole-3-carbonyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines to form indole-based amides, which are key structural motifs in bioactive molecules. Commonly employed in the development of serotonin receptor ligands and other neuroactive compounds due to the indole core’s prevalence in neurotransmitters. Also utilized in the preparation of fluorescent probes and dyes, where the indole scaffold contributes to light absorpt

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines to form indole-based amides, which are key structural motifs in bioactive molecules. Commonly employed in the development of serotonin receptor ligands and other neuroactive compounds due to the indole core’s prevalence in neurotransmitters. Also utilized in the preparation of fluorescent probes and dyes, where the indole scaffold contributes to light absorption and emission properties. Its reactivity allows for efficient derivatization in combinatorial chemistry and drug discovery pipelines.

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