4-(1-Methyl-1H-pyrazol-3-yl)benzaldehyde

96%

Reagent Code: #208772
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CAS Number 179055-27-7

science Other reagents with same CAS 179055-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.21 g/mol
Formula C₁₁H₁₀N₂O
badge Registry Numbers
MDL Number MFCD08669906
thermostat Physical Properties
Melting Point 97.5°C
Boiling Point 350.2°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, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its aromatic and heterocyclic properties. Commonly utilized in cross-coupling reactions and condensation processes to build complex molecules in research laboratories.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,950.00
inventory 250mg
10-20 days ฿7,030.00
inventory 1g
10-20 days ฿18,970.00

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4-(1-Methyl-1H-pyrazol-3-yl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its aromatic and heterocyclic properties. Commonly utilized in cross-coupling reactions and condensation processes to build complex molecules in research laboratories.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its aromatic and heterocyclic properties. Commonly utilized in cross-coupling reactions and condensation processes to build complex molecules in research laboratories.

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