Ethyl 5-bromo-1-methyl-1H-pyrazole-4-carboxylate

95%

Reagent Code: #84118
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CAS Number 105486-72-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.06 g/mol
Formula C₇H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD13189831
inventory_2 Storage & Handling
Storage room temperature, inert atmosphere

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the production of various heterocyclic compounds. Its structure, featuring both a bromo and an ester functional group, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. Specifically, it is often employed in the synthesis of pyrazole derivatives, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, the compound is used in research settings to explore novel chemical reactions and to develop new methodologies in medicinal chemistry. Its reactivity allows for further functionalization, enabling the creation of diverse molecular structures with potential therapeutic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,692.00
inventory 1g
10-20 days ฿5,220.00
inventory 5g
10-20 days ฿20,700.00
Ethyl 5-bromo-1-methyl-1H-pyrazole-4-carboxylate
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the production of various heterocyclic compounds. Its structure, featuring both a bromo and an ester functional group, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. Specifically, it is often employed in the synthesis of pyrazole derivatives, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, the compound is used in research settings to explore novel chemical reactions and to develop new methodologies in medicinal chemistry. Its reactivity allows for further functionalization, enabling the creation of diverse molecular structures with potential therapeutic applications.
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