2-Bromo-3-methylphenol

98%

Reagent Code: #145022
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CAS Number 22061-78-5

science Other reagents with same CAS 22061-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.03 g/mol
Formula C₇H₇BrO
thermostat Physical Properties
Boiling Point 215.2°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of more complex organic molecules where the bromo and hydroxyl functional groups allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of specialty chemicals including fragrances and antioxidants due to its phenolic structure. Its reactivity makes it valuable in research laboratories for building substituted aromatic compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿150.00
inventory 1g
10-20 days ฿330.00
inventory 25g
10-20 days ฿6,130.00
inventory 100g
10-20 days ฿23,890.00
inventory 5g
10-20 days ฿1,270.00

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2-Bromo-3-methylphenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of more complex organic molecules where the bromo and hydroxyl functional groups allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of specialty chemicals including fragrances and antioxidants due to its phenolic structure. Its reactivity makes it valuable in research

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of more complex organic molecules where the bromo and hydroxyl functional groups allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of specialty chemicals including fragrances and antioxidants due to its phenolic structure. Its reactivity makes it valuable in research laboratories for building substituted aromatic compounds.

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