Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

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Reagent Code: #182781
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CAS Number 1436686-17-7

science Other reagents with same CAS 1436686-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.08 g/mol
Formula C₉H₈BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high specificity. Also employed in agrochemical research to create novel pesticides with improved efficacy and environmental safety. Commonly utilized in combinatorial chemistry and high-throughput screening due to its reactive bromine moiety, which allows for easy functionalization via cross-coupling reactions such as Suzuki or Heck reactions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿650.00
inventory 100mg
10-20 days ฿760.00
inventory 250mg
10-20 days ฿1,720.00
inventory 1g
10-20 days ฿6,860.00

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Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high specificity. Also employed in agrochemical research to create novel pesticides with improved efficacy and environmental safety. Commonly utilized in combinatorial chemistry and high-throughput screening due to its react

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high specificity. Also employed in agrochemical research to create novel pesticides with improved efficacy and environmental safety. Commonly utilized in combinatorial chemistry and high-throughput screening due to its reactive bromine moiety, which allows for easy functionalization via cross-coupling reactions such as Suzuki or Heck reactions.

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