2-Chloro-9-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde

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Reagent Code: #163278
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CAS Number 17326-27-1

science Other reagents with same CAS 17326-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.63 g/mol
Formula C₁₀H₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD03284432
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

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 enables functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its conjugated system, which can be modified to detect specific biomolecules. Additionally, it serves as a building block in the design of novel heterocyclic compounds for drug discovery research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,660.00
inventory 250mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿7,370.00

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2-Chloro-9-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-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 enables functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its conjugated system, which can be modified to detect specific biomolecules. Additionally, it serves as a building block in the design

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its conjugated system, which can be modified to detect specific biomolecules. Additionally, it serves as a building block in the design of novel heterocyclic compounds for drug discovery research.

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