2-Bromobenzene-1,3,5-triol

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Reagent Code: #146299
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CAS Number 84743-77-1

science Other reagents with same CAS 84743-77-1

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scatter_plot Molecular Information
Weight 205.01 g/mol
Formula C₆H₅BrO₃
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MDL Number MFCD22056138
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive bromine group allows for coupling reactions, such as Suzuki or Ullmann reactions, enabling the construction of complex aromatic structures. Also employed in the development of dyes and UV absorbers due to its phenolic structure, which provides stability and light absorption properties. Additionally, it has been explored in the synthesis of antioxidants and bioactive molecules owing to the triol functionality, which can participate in hydrogen bonding and chelation.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿120.00
inventory 250mg
10-20 days ฿444.00
inventory 1g
10-20 days ฿2,740.00

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2-Bromobenzene-1,3,5-triol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive bromine group allows for coupling reactions, such as Suzuki or Ullmann reactions, enabling the construction of complex aromatic structures. Also employed in the development of dyes and UV absorbers due to its phenolic structure, which provides stability and light absorption properties. Additionally, it has been explored in the synthesis of antioxidants and bioactive molecules

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive bromine group allows for coupling reactions, such as Suzuki or Ullmann reactions, enabling the construction of complex aromatic structures. Also employed in the development of dyes and UV absorbers due to its phenolic structure, which provides stability and light absorption properties. Additionally, it has been explored in the synthesis of antioxidants and bioactive molecules owing to the triol functionality, which can participate in hydrogen bonding and chelation.

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