Ethyl 5-amino-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate

≥95%

Reagent Code: #183516
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CAS Number 618070-65-8

science Other reagents with same CAS 618070-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.24 g/mol
Formula C₁₂H₁₂FN₃O₂
badge Registry Numbers
MDL Number MFCD03407403
thermostat Physical Properties
Boiling Point 386.4±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the formation of biologically active molecules targeting central nervous system disorders and certain cancers. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in research settings for generating novel pyrazole-based derivatives with potential therapeutic activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿350.00
inventory 1g
10-20 days ฿1,130.00
inventory 5g
10-20 days ฿5,630.00

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Ethyl 5-amino-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the formation of biologically active molecules targeting central nervous system disorders and certain cancers. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in research settings for generating novel pyrazole-based derivatives with potential therapeutic a

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the formation of biologically active molecules targeting central nervous system disorders and certain cancers. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in research settings for generating novel pyrazole-based derivatives with potential therapeutic activity.

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