Ethyl 5-aminoopyrazolo[1,5-a]pyridine-3-carboxylate

≥95%

Reagent Code: #183480
label
Alias 5-aminopyrazolo[1,5-A]pyridine-3-carboxylic acid ethyl ester; 5-Aminoopyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester
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CAS Number 1101120-35-7

science Other reagents with same CAS 1101120-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.220 g/mol
Formula C₁₀H₁₁N₃O₂
badge Registry Numbers
MDL Number MFCD20923175
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of biologically active compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its favorable photophysical properties. Serves as a building block in agrochemicals for designing novel pesticides with improved efficacy.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿24,000.00
inventory 10g
10-20 days ฿48,000.00
inventory 25g
10-20 days ฿96,000.00
inventory 1g
10-20 days ฿8,000.00

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Ethyl 5-aminoopyrazolo[1,5-a]pyridine-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 cancer treatment. Its structure supports the formation of biologically active compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its favorable photophysical properties. Serves as a building block in agrochemi

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of biologically active compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its favorable photophysical properties. Serves as a building block in agrochemicals for designing novel pesticides with improved efficacy.

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