4-Bromocatechol

≥98.0%

Reagent Code: #143612
label
Alias 4-bromo-1,2-dihydroxybenzene; 4-bromo-1,2-phenylphenol
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CAS Number 17345-77-6

science Other reagents with same CAS 17345-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.01 g/mol
Formula C₆H₅BrO₂
badge Registry Numbers
MDL Number MFCD00869769
thermostat Physical Properties
Melting Point 87 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilators and agents for treating cardiovascular conditions. It serves as a building block in organic synthesis due to the presence of both hydroxyl and bromo functional groups, enabling selective reactions for constructing complex molecules. Also employed in the development of agrochemicals and specialty polymers where halogenated aromatic structures are required. Its reactivity allows for cross-coupling reactions, making it valuable in research and industrial applications for creating biologically active compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿1,870.00
inventory 25g
10-20 days ฿5,670.00
inventory 100g
10-20 days ฿22,000.00

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4-Bromocatechol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilators and agents for treating cardiovascular conditions. It serves as a building block in organic synthesis due to the presence of both hydroxyl and bromo functional groups, enabling selective reactions for constructing complex molecules. Also employed in the development of agrochemicals and specialty polymers where halogenated aromatic structures are required. Its reactivity allows for cross-coupling

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilators and agents for treating cardiovascular conditions. It serves as a building block in organic synthesis due to the presence of both hydroxyl and bromo functional groups, enabling selective reactions for constructing complex molecules. Also employed in the development of agrochemicals and specialty polymers where halogenated aromatic structures are required. Its reactivity allows for cross-coupling reactions, making it valuable in research and industrial applications for creating biologically active compounds.

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