3-Bromo-1,5-dimethyl-1H-pyrazole-4-carbaldehyde

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Reagent Code: #148405
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CAS Number 1557804-67-7

science Other reagents with same CAS 1557804-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.04 g/mol
Formula C₆H₇BrN₂O
thermostat Physical Properties
Boiling Point 284.2±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in 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 scaffolds. Its functional groups enable selective derivatization, making it valuable in constructing heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions to introduce the pyrazole core into larger molecular structures with desired biological activity. Also utilized in research settings for the preparation of novel insecticides and fungicides due to the inherent stability and reactivity of the brominated pyrazole ring.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,500.00
inventory 1g
10-20 days ฿12,670.00

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3-Bromo-1,5-dimethyl-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 scaffolds. Its functional groups enable selective derivatization, making it valuable in constructing heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions to introduce the pyrazole core into larger molecular structures with desired biological activity. Also utilized in research settings for the preparation of novel insect

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole scaffolds. Its functional groups enable selective derivatization, making it valuable in constructing heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions to introduce the pyrazole core into larger molecular structures with desired biological activity. Also utilized in research settings for the preparation of novel insecticides and fungicides due to the inherent stability and reactivity of the brominated pyrazole ring.

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