4-Bromo-3-(tert-butyl)phenol

≥95%

Reagent Code: #141690
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CAS Number 103414-68-2

science Other reagents with same CAS 103414-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.1136 g/mol
Formula C₁₀H₁₃BrO
badge Registry Numbers
MDL Number MFCD15527202
thermostat Physical Properties
Boiling Point 277.1±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.341±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of both bromo and phenolic functional groups, enabling cross-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the preparation of antioxidants and stabilizers for polymers and industrial materials. Its tert-butyl group contributes to steric hindrance, enhancing selectivity in synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,000.00
inventory 5g
10-20 days ฿22,400.00
inventory 10g
10-20 days ฿36,800.00
inventory 25g
10-20 days ฿73,600.00

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4-Bromo-3-(tert-butyl)phenol
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of both bromo and phenolic functional groups, enabling cross-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the preparation of antioxidants and stabilizers for polymers and industrial materials. Its tert-butyl group contributes to steric hindrance, enhancing selectivity

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of both bromo and phenolic functional groups, enabling cross-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the preparation of antioxidants and stabilizers for polymers and industrial materials. Its tert-butyl group contributes to steric hindrance, enhancing selectivity in synthetic pathways.

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