1H-Pyrazole-5-carboxaldehyde

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Reagent Code: #194825
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CAS Number 948552-36-1

science Other reagents with same CAS 948552-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 96.09 g/mol
Formula C₄H₄N₂O
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with anti-inflammatory, analgesic, and antimicrobial properties. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its reactive aldehyde group that allows functionalization. Also employed in the preparation of dyes and functional materials where heterocyclic frameworks enhance electronic or optical properties. Its versatility in cross-coupling and condensation reactions makes it valuable in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,330.00
inventory 5g
10-20 days ฿9,600.00
inventory 25g
10-20 days ฿38,920.00

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1H-Pyrazole-5-carboxaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with anti-inflammatory, analgesic, and antimicrobial properties. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its reactive aldehyde group that allows functionalization. Also employed in the preparation of dyes and functional materials where heterocyclic frameworks enhance electronic or optical properties. Its versatility in cross-coupling

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with anti-inflammatory, analgesic, and antimicrobial properties. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its reactive aldehyde group that allows functionalization. Also employed in the preparation of dyes and functional materials where heterocyclic frameworks enhance electronic or optical properties. Its versatility in cross-coupling and condensation reactions makes it valuable in medicinal chemistry research and development.

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