6-Methoxy-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde

95%

Reagent Code: #50074
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CAS Number 944900-73-6

science Other reagents with same CAS 944900-73-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.1720 g/mol
Formula C₉H₈N₂O₂
badge Registry Numbers
MDL Number MFCD10697641
inventory_2 Storage & Handling
Density 1.347g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, including potential drugs targeting neurological disorders and cancer. Researchers leverage its aldehyde functional group to facilitate coupling reactions, enabling the creation of complex molecules with therapeutic potential. Additionally, it serves as a building block in the design of heterocyclic compounds, which are often explored for their pharmacological properties. Its applications extend to the study of enzyme inhibition and receptor modulation, making it a versatile tool in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,056.00

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6-Methoxy-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, including potential drugs targeting neurological disorders and cancer. Researchers leverage its aldehyde functional group to facilitate coupling reactions, enabling the creation of complex molecules with therapeutic potential. Additionally, it serves as a building block i

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, including potential drugs targeting neurological disorders and cancer. Researchers leverage its aldehyde functional group to facilitate coupling reactions, enabling the creation of complex molecules with therapeutic potential. Additionally, it serves as a building block in the design of heterocyclic compounds, which are often explored for their pharmacological properties. Its applications extend to the study of enzyme inhibition and receptor modulation, making it a versatile tool in drug discovery and development.

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