4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

97%

Reagent Code: #45849
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CAS Number 4492-02-8

science Other reagents with same CAS 4492-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.23 g/mol
Formula C₁₀H₁₄N₂O₂
thermostat Physical Properties
Melting Point 88 ℃
Boiling Point 403.5±45.0 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.06g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. It serves as a building block for creating compounds that target specific enzymes or receptors, particularly in the development of potential therapeutic agents. Its structural features make it valuable in designing inhibitors for kinases, which are crucial in regulating cellular processes and signaling pathways. Additionally, it is explored in the synthesis of heterocyclic compounds that may exhibit anti-inflammatory, anticancer, or antimicrobial properties. Its ethyl ester group enhances its reactivity and solubility, facilitating its use in organic synthesis and medicinal chemistry applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,281.00
inventory 1g
10-20 days ฿2,358.00
inventory 25g
10-20 days ฿28,800.00

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4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER
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This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. It serves as a building block for creating compounds that target specific enzymes or receptors, particularly in the development of potential therapeutic agents. Its structural features make it valuable in designing inhibitors for kinases, which are crucial in regulating cellular processes and signaling pathways. Additionally, it is explored in the synthesis of heterocyclic compounds that may exhibit anti-inflammatory, anticancer, or antimicrobial properties. Its ethyl ester group enhances its reactivity and solubility, facilitating its use in organic synthesis and medicinal chemistry applications.
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