3-Bromo-1-methyl-1H-pyrazole-4-carbaldehyde

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Reagent Code: #141115
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CAS Number 1368167-47-8

science Other reagents with same CAS 1368167-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.01 g/mol
Formula C₅H₅N₂OBr
badge Registry Numbers
MDL Number MFCD22062890
thermostat Physical Properties
Boiling Point 275.2±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.73±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole cores. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic compounds. Commonly employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents. Also utilized in the preparation of crop protection agents due to the biological activity associated with substituted pyrazoles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,900.00
inventory 250mg
10-20 days ฿20,220.00
inventory 1g
10-20 days ฿54,560.00

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3-Bromo-1-methyl-1H-pyrazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole cores. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic compounds. Commonly employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents. Also utilized in the preparation of

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole cores. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex heterocyclic compounds. Commonly employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents. Also utilized in the preparation of crop protection agents due to the biological activity associated with substituted pyrazoles.

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