3-Chloro-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde

98%

Reagent Code: #156661
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CAS Number 1190309-77-3

science Other reagents with same CAS 1190309-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.59 g/mol
Formula C₈H₅N₂OCl
badge Registry Numbers
MDL Number MFCD12962907
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in creating targeted therapies. It is also employed in the preparation of biologically active heterocyclic compounds, especially those with antiviral or anti-inflammatory properties. Due to the presence of reactive aldehyde and halogen groups, it serves as a versatile building block in medicinal chemistry for forming carbon-carbon and carbon-nitrogen bonds through cross-coupling and condensation reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,530.00
inventory 1g
10-20 days ฿62,070.00

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3-Chloro-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in creating targeted therapies. It is also employed in the preparation of biologically active heterocyclic compounds, especially those with antiviral or anti-inflammatory properties. Due to the presence of reactive aldehyde and halogen groups, it serves as a versatile building block in m

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in creating targeted therapies. It is also employed in the preparation of biologically active heterocyclic compounds, especially those with antiviral or anti-inflammatory properties. Due to the presence of reactive aldehyde and halogen groups, it serves as a versatile building block in medicinal chemistry for forming carbon-carbon and carbon-nitrogen bonds through cross-coupling and condensation reactions.

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