Ethyl 4-Bromo-1,5-dimethyl-1H-pyrazole-3-carboxylate

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Reagent Code: #184255
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CAS Number 5775-90-6

science Other reagents with same CAS 5775-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.09 g/mol
Formula C₈H₁₁BrN₂O₂
badge Registry Numbers
MDL Number MFCD00207970
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and analgesic properties. Its structure, featuring a bromine substituent at the 4-position and an ethyl carboxylate ester at the 3-position of the 1,5-dimethyl-1H-pyrazole ring, allows for further functionalization through reactions such as nucleophilic substitution at the bromine or hydrolysis/saponification of the ester group, enabling tailoring of chemical and biological properties. This makes it valuable in medicinal chemistry for constructing pyrazole-based compounds. It is also employed in research settings to design novel heterocyclic systems for drug discovery and crop protection agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,870.00
inventory 5g
10-20 days ฿9,330.00
inventory 10g
10-20 days ฿17,280.00
inventory 250mg
10-20 days ฿1,180.00

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Ethyl 4-Bromo-1,5-dimethyl-1H-pyrazole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and analgesic properties. Its structure, featuring a bromine substituent at the 4-position and an ethyl carboxylate ester at the 3-position of the 1,5-dimethyl-1H-pyrazole ring, allows for further functionalization through reactions such as nucleophilic substitution at the bromine or hydrolysis/saponification of the ester group, en

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and analgesic properties. Its structure, featuring a bromine substituent at the 4-position and an ethyl carboxylate ester at the 3-position of the 1,5-dimethyl-1H-pyrazole ring, allows for further functionalization through reactions such as nucleophilic substitution at the bromine or hydrolysis/saponification of the ester group, enabling tailoring of chemical and biological properties. This makes it valuable in medicinal chemistry for constructing pyrazole-based compounds. It is also employed in research settings to design novel heterocyclic systems for drug discovery and crop protection agents.

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