Methyl 4-bromo-1H-indole-6-carboxylate

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Reagent Code: #207006
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CAS Number 882679-96-1

science Other reagents with same CAS 882679-96-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
badge Registry Numbers
MDL Number MFCD03867040
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. Commonly employed in the development of serotonin receptor modulators and other neuroactive compounds. Its bromo functional group allows for further cross-coupling reactions, making it valuable in constructing complex molecules for drug discovery. Also utilized in the preparation of tryptamine and tryptophan analogs with potential antitumor, antiviral, or psychotropic activity. Frequently appears in studies involving palladium-catalyzed coupling reactions to expand molecular diversity in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿280.00
inventory 1g
10-20 days ฿247.50
inventory 5g
10-20 days ฿1,880.00
inventory 25g
10-20 days ฿8,610.00

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Methyl 4-bromo-1H-indole-6-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. Commonly employed in the development of serotonin receptor modulators and other neuroactive compounds. Its bromo functional group allows for further cross-coupling reactions, making it valuable in constructing complex molecules for drug discovery. Also utilized in the preparation of tryptamine and tryptophan analogs with potential antitumor, antiviral, or psychotropic activity. Frequently appears in st

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. Commonly employed in the development of serotonin receptor modulators and other neuroactive compounds. Its bromo functional group allows for further cross-coupling reactions, making it valuable in constructing complex molecules for drug discovery. Also utilized in the preparation of tryptamine and tryptophan analogs with potential antitumor, antiviral, or psychotropic activity. Frequently appears in studies involving palladium-catalyzed coupling reactions to expand molecular diversity in medicinal chemistry.

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