1-(Benzenesulfonyl)-4-bromo-1H-pyrrolo[2,3-b]pyridine

98%

Reagent Code: #150590
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CAS Number 889939-25-7

science Other reagents with same CAS 889939-25-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.19 g/mol
Formula C₁₃H₉BrN₂O₂S
badge Registry Numbers
MDL Number MFCD08443800
thermostat Physical Properties
Boiling Point 511.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors and other drug candidates targeting cancer and inflammatory diseases. The bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituents. Its sulfonyl moiety enhances stability and influences binding affinity in medicinal chemistry applications. Commonly employed in the development of small molecule therapeutics through structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿750.00
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿3,180.00
inventory 5g
10-20 days ฿15,670.00
inventory 25g
10-20 days ฿68,060.00

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1-(Benzenesulfonyl)-4-bromo-1H-pyrrolo[2,3-b]pyridine
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors and other drug candidates targeting cancer and inflammatory diseases. The bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituents. Its sulfonyl moiety enhances stability and influences binding affinity in medicinal chemistry applications. Commonly employed in the development of

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors and other drug candidates targeting cancer and inflammatory diseases. The bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituents. Its sulfonyl moiety enhances stability and influences binding affinity in medicinal chemistry applications. Commonly employed in the development of small molecule therapeutics through structure-activity relationship studies.

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