Methyl 6-bromo-1-(sec-butyl)-1H-indole-4-carboxylate

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Reagent Code: #210548
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CAS Number 1346576-37-1

science Other reagents with same CAS 1346576-37-1

blur_circular Chemical Specifications

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Weight 310.19 g/mol
Formula C₁₄H₁₆BrNO₂
badge Registry Numbers
MDL Number MFCD28386916
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of bioactive indole derivatives. Shows potential in the development of central nervous system agents due to the indole core’s affinity for neurotransmitter receptors. Employed in medicinal chemistry for structure-activity relationship studies, particularly in optimizing substituents for enhanced potency and selectivity. Also applied in the preparation of analogs for anticancer and anti-inflammatory screening. Its bromo functionality allows for further cross-coupling reactions, making it valuable in building complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,960.00
inventory 250mg
10-20 days ฿11,110.00
inventory 1g
10-20 days ฿28,800.00

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Methyl 6-bromo-1-(sec-butyl)-1H-indole-4-carboxylate
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Used in pharmaceutical research as an intermediate in the synthesis of bioactive indole derivatives. Shows potential in the development of central nervous system agents due to the indole core’s affinity for neurotransmitter receptors. Employed in medicinal chemistry for structure-activity relationship studies, particularly in optimizing substituents for enhanced potency and selectivity. Also applied in the preparation of analogs for anticancer and anti-inflammatory screening. Its bromo functionality allo

Used in pharmaceutical research as an intermediate in the synthesis of bioactive indole derivatives. Shows potential in the development of central nervous system agents due to the indole core’s affinity for neurotransmitter receptors. Employed in medicinal chemistry for structure-activity relationship studies, particularly in optimizing substituents for enhanced potency and selectivity. Also applied in the preparation of analogs for anticancer and anti-inflammatory screening. Its bromo functionality allows for further cross-coupling reactions, making it valuable in building complex molecular architectures.

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