(2-Bromo-5-methoxyphenyl)methanol

95%

Reagent Code: #113123
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CAS Number 150192-39-5

science Other reagents with same CAS 150192-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.06 g/mol
Formula C₈H₉BrO₂
badge Registry Numbers
MDL Number MFCD03695463
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

(2-Bromo-5-methoxyphenyl)methanol is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a key building block in the development of complex molecules due to its reactive bromine and hydroxyl groups. The compound is often employed in coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it finds application in the synthesis of agrochemicals and materials science, where its structural features contribute to the design of novel polymers or functional materials. Its versatility in chemical transformations makes it valuable in research and industrial settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,142.00
inventory 5g
10-20 days ฿5,994.00
inventory 250mg
10-20 days ฿1,512.00

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(2-Bromo-5-methoxyphenyl)methanol
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(2-Bromo-5-methoxyphenyl)methanol is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a key building block in the development of complex molecules due to its reactive bromine and hydroxyl groups. The compound is often employed in coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it finds application in the synthesis of agrochemicals and materials

(2-Bromo-5-methoxyphenyl)methanol is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a key building block in the development of complex molecules due to its reactive bromine and hydroxyl groups. The compound is often employed in coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it finds application in the synthesis of agrochemicals and materials science, where its structural features contribute to the design of novel polymers or functional materials. Its versatility in chemical transformations makes it valuable in research and industrial settings.

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