4-Bromo-7-methyl-1H-benzo[d][1,2,3]triazole

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Reagent Code: #140929
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CAS Number 1388070-71-0

science Other reagents with same CAS 1388070-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.05 g/mol
Formula C₇H₆BrN₃
badge Registry Numbers
MDL Number MFCD23838739
thermostat Physical Properties
Boiling Point 420.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.755±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules targeting kinase inhibition. Its bromo and triazole functionalities allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce aryl or amino groups. Also applied in materials science for designing fluorescent probes and corrosion inhibitors due to its electron-rich aromatic structure and metal-coordinating ability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,320.00
inventory 1g
10-20 days ฿83,690.00

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4-Bromo-7-methyl-1H-benzo[d][1,2,3]triazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules targeting kinase inhibition. Its bromo and triazole functionalities allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce aryl or amino groups. Also applied in materials science for designing fluorescent probes and corrosio

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules targeting kinase inhibition. Its bromo and triazole functionalities allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce aryl or amino groups. Also applied in materials science for designing fluorescent probes and corrosion inhibitors due to its electron-rich aromatic structure and metal-coordinating ability.

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