1-Acetyl-3-Hydroxy-1H-Pyrazole-4-Carboxylic Acid Ethyl Ester

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Reagent Code: #137769
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CAS Number 478968-45-5

science Other reagents with same CAS 478968-45-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.17 g/mol
Formula C₈H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD13689094
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the formation of pyrazole-based derivatives, which are known for their biological activity. It is also employed in research settings to design new heterocyclic compounds with potential therapeutic applications. The ester and hydroxyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,560.00
inventory 250mg
10-20 days ฿19,270.00

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1-Acetyl-3-Hydroxy-1H-Pyrazole-4-Carboxylic Acid Ethyl Ester
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the formation of pyrazole-based derivatives, which are known for their biological activity. It is also employed in research settings to design new heterocyclic compounds with potential therapeutic applications. The ester and hydroxyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for s
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the formation of pyrazole-based derivatives, which are known for their biological activity. It is also employed in research settings to design new heterocyclic compounds with potential therapeutic applications. The ester and hydroxyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.
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