6-Chloro-3-methylimidazo[1,2-b]pyridazine

98%

Reagent Code: #160691
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CAS Number 137384-48-6

science Other reagents with same CAS 137384-48-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.6 g/mol
Formula C₇H₆ClN₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key 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 ability to enhance binding affinity with biological targets. Commonly employed in the preparation of compounds targeting inflammatory diseases and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its structure supports the optimization of drug-like properties such as metabolic stability and solubility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,760.00
inventory 1g
10-20 days ฿6,120.00

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6-Chloro-3-methylimidazo[1,2-b]pyridazine
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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. It serves as a building block in medicinal chemistry due to its ability to enhance binding affinity with biological targets. Commonly employed in the preparation of compounds targeting inflammatory diseases and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its st

Used as a key 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 ability to enhance binding affinity with biological targets. Commonly employed in the preparation of compounds targeting inflammatory diseases and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its structure supports the optimization of drug-like properties such as metabolic stability and solubility.

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