4-Bromo-5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine

97%

Reagent Code: #155485
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CAS Number 1245646-53-0

science Other reagents with same CAS 1245646-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 382.19 g/mol
Formula C₁₃H₈BrN₃O₄S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of anticancer agents due to its ability to participate in cross-coupling reactions, enabling the introduction of various functional groups. Commonly employed in medicinal chemistry for constructing pyrrolopyridine-based scaffolds, which are known for their enzyme inhibitory properties. Also utilized in the preparation of fluorescent probes and agrochemicals owing to its electron-withdrawing nitro and bromo groups that facilitate further derivatization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿7,510.00
1g
10-20 days ฿20,860.00
5g
10-20 days ฿76,550.00
100mg
10-20 days ฿3,770.00
4-Bromo-5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of anticancer agents due to its ability to participate in cross-coupling reactions, enabling the introduction of various functional groups. Commonly employed in medicinal chemistry for constructing pyrrolopyridine-based scaffolds, which are known for their enzyme inhibitory properties. Also utilized in the preparation of

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of anticancer agents due to its ability to participate in cross-coupling reactions, enabling the introduction of various functional groups. Commonly employed in medicinal chemistry for constructing pyrrolopyridine-based scaffolds, which are known for their enzyme inhibitory properties. Also utilized in the preparation of fluorescent probes and agrochemicals owing to its electron-withdrawing nitro and bromo groups that facilitate further derivatization.

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