2,4-dichloroquinazoline

≥95%

Reagent Code: #170114
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CAS Number 607-68-1

science Other reagents with same CAS 607-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.04 g/mol
Formula C₈H₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD00091950
inventory_2 Storage & Handling
Storage -20℃, drying, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. It serves as a building block for compounds with biological activity, including those targeting tyrosine kinases involved in tumor growth. Also employed in the preparation of agrochemicals and dyes due to its reactive halogen sites, which allow for further functionalization through nucleophilic substitution reactions. Its structure supports the design of molecules with enhanced binding affinity to specific enzyme active sites.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿750.00
inventory 25g
10-20 days ฿3,250.00
inventory 100g
10-20 days ฿11,900.00

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2,4-dichloroquinazoline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. It serves as a building block for compounds with biological activity, including those targeting tyrosine kinases involved in tumor growth. Also employed in the preparation of agrochemicals and dyes due to its reactive halogen sites, which allow for further functionalization through nucleophilic substitution reactions. Its structure supports the design of molecules wi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. It serves as a building block for compounds with biological activity, including those targeting tyrosine kinases involved in tumor growth. Also employed in the preparation of agrochemicals and dyes due to its reactive halogen sites, which allow for further functionalization through nucleophilic substitution reactions. Its structure supports the design of molecules with enhanced binding affinity to specific enzyme active sites.

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