4-(6-Chloropyridazin-3-yl)benzaldehyde

95%

Reagent Code: #160603
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CAS Number 914349-19-2

science Other reagents with same CAS 914349-19-2

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scatter_plot Molecular Information
Weight 218.64 g/mol
Formula C₁₁H₇ClN₂O
badge Registry Numbers
MDL Number MFCD05864739
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heteroaromatic structure, enabling coupling reactions and ring formations. Also employed in agrochemical research for designing novel pesticides with targeted activity. Its chloropyridazine moiety contributes to enhanced binding affinity in biological systems, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,010.00
inventory 1g
10-20 days ฿9,980.00

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4-(6-Chloropyridazin-3-yl)benzaldehyde
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heteroaromatic structure, enabling coupling reactions and ring formations. Also employed in agrochemical research for designing novel pesticides with targeted activity. Its chloropyridazine moiety contributes to enhanced binding affinity in biological systems, making it v

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heteroaromatic structure, enabling coupling reactions and ring formations. Also employed in agrochemical research for designing novel pesticides with targeted activity. Its chloropyridazine moiety contributes to enhanced binding affinity in biological systems, making it valuable in structure-activity relationship studies.

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