6-Chloroimidazo[1,2-b]pyridazine-3-carbonitrile

95%

Reagent Code: #173608
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CAS Number 123531-54-4

science Other reagents with same CAS 123531-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.58 g/mol
Formula C₇H₃ClN₄
badge Registry Numbers
MDL Number MFCD11044763
inventory_2 Storage & Handling
Storage Room temperature, dry

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 participate in cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic systems. Its nitrile and chloro functionalities allow for selective modifications, making it valuable in optimizing drug candidates for improved potency and selectivity. Also employed in agrochemical research for designing novel bioactive molecules with potential pesticidal or herbicidal activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,590.00
inventory 5g
10-20 days ฿49,200.00
inventory 10g
10-20 days ฿85,550.00
inventory 250mg
10-20 days ฿5,430.00

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6-Chloroimidazo[1,2-b]pyridazine-3-carbonitrile
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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 participate in cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic systems. Its nitrile and chloro functionalities allow for selective modifications, making it valuable in optimizing drug candidates for improved potency and selecti

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 participate in cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic systems. Its nitrile and chloro functionalities allow for selective modifications, making it valuable in optimizing drug candidates for improved potency and selectivity. Also employed in agrochemical research for designing novel bioactive molecules with potential pesticidal or herbicidal activity.

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