4-bromo-2-(2-hydroxyethyl)phenol

95%

Reagent Code: #150809
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CAS Number 198277-06-4

science Other reagents with same CAS 198277-06-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.06 g/mol
Formula C₈H₉BrO₂
badge Registry Numbers
MDL Number MFCD09907900
thermostat Physical Properties
Boiling Point 328.8±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.615±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of drugs requiring brominated aromatic structures for further functionalization. Its hydroxyl and bromo groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of UV absorbers and antioxidants for polymers due to its phenolic structure. Also utilized in the production of specialty resins and as a building block in agrochemical synthesis. Its reactivity supports use in cross-coupling reactions, enabling the formation of carbon-carbon bonds in advanced organic manufacturing processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,320.00
inventory 250mg
10-20 days ฿29,740.00
inventory 1g
10-20 days ฿59,410.00

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4-bromo-2-(2-hydroxyethyl)phenol
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of drugs requiring brominated aromatic structures for further functionalization. Its hydroxyl and bromo groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of UV absorbers and antioxidants for polymers due to its phenolic structure. Also utilized in the production of specialty resins and as a building block in agro

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of drugs requiring brominated aromatic structures for further functionalization. Its hydroxyl and bromo groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of UV absorbers and antioxidants for polymers due to its phenolic structure. Also utilized in the production of specialty resins and as a building block in agrochemical synthesis. Its reactivity supports use in cross-coupling reactions, enabling the formation of carbon-carbon bonds in advanced organic manufacturing processes.

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