Ethyl 2-(3-chloropyridin-2-yl)-5-oxopyrazolidine-3-carboxylate

95%

Reagent Code: #184300
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CAS Number 500011-88-1

science Other reagents with same CAS 500011-88-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.68 g/mol
Formula C₁₁H₁₂ClN₃O₃
badge Registry Numbers
MDL Number MFCD09955582
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

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 supports the formation of biologically active molecules with high selectivity. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its favorable reactivity and ability to participate in further functionalization reactions. Also utilized in the preparation of pyridinylpyrazole derivatives, which exhibit anti-inflammatory and antimicrobial properties. Suitable for use in combinatorial chemistry and high-throughput screening for new drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿3,100.00
inventory 5g
10-20 days ฿10,850.00
inventory 25g
10-20 days ฿36,850.00
inventory 100g
10-20 days ฿113,500.00

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Ethyl 2-(3-chloropyridin-2-yl)-5-oxopyrazolidine-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 supports the formation of biologically active molecules with high selectivity. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its favorable reactivity and ability to participate in further functionalization reactions. Also utilized in the preparation of pyridinylpyrazole derivatives, which exhibit a

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the formation of biologically active molecules with high selectivity. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its favorable reactivity and ability to participate in further functionalization reactions. Also utilized in the preparation of pyridinylpyrazole derivatives, which exhibit anti-inflammatory and antimicrobial properties. Suitable for use in combinatorial chemistry and high-throughput screening for new drug discovery.

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