Ethyl 5-((tert-Butoxycarbonyl)amino)pyrazolo[1,5-a]pyridine-3-carboxylate

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Reagent Code: #183481
label
Alias Ethyl 5-(tert-butoxycarbonylamino)pyrazolo[1,5-A]pyridine-3-carboxylate
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CAS Number 1101120-33-5

science Other reagents with same CAS 1101120-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.3400 g/mol
Formula C₁₅H₁₉N₃O₄
badge Registry Numbers
MDL Number MFCD21099564
inventory_2 Storage & Handling
Density 1.23g/ml
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the construction of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research for optimizing lead compounds due to its favorable reactivity and stability in multi-step synthesis. Also utilized in the preparation of pyrazolopyridine-based drug candidates targeting inflammatory and neurological disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,800.00
inventory 1g
10-20 days ฿15,810.00
inventory 50mg
10-20 days ฿4,610.00

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Ethyl 5-((tert-Butoxycarbonyl)amino)pyrazolo[1,5-a]pyridine-3-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the construction of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research for optimizing lead compounds due to its favorable reactivity and stability in multi-step synthesis. Also utilized in the preparation of pyrazolopyridine-based drug candidates targeting inflammatory and neur

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the construction of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research for optimizing lead compounds due to its favorable reactivity and stability in multi-step synthesis. Also utilized in the preparation of pyrazolopyridine-based drug candidates targeting inflammatory and neurological disorders.

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