4,7-Dichlorofuro[2,3-d]pyridazine

98%

Reagent Code: #178144
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CAS Number 13177-70-3

science Other reagents with same CAS 13177-70-3

blur_circular Chemical Specifications

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Weight 189.00 g/mol
Formula C₆H₂Cl₂N₂O
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MDL Number MFCD08692049
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 allows for selective binding to enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental safety. Commonly utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen sites, which enable further functionalization through cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,640.00
inventory 250mg
10-20 days ฿18,080.00
inventory 1g
10-20 days ฿38,240.00

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4,7-Dichlorofuro[2,3-d]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. Its structure allows for selective binding to enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental safety. Commonly utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen sites, which enable further func

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding to enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental safety. Commonly utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen sites, which enable further functionalization through cross-coupling reactions.

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