Methyl 3-bromo-2,6-dimethylbenzoate

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Reagent Code: #45144
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CAS Number 86246-71-1

science Other reagents with same CAS 86246-71-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.10 g/mol
Formula C₁₀H₁₁BrO₂
badge Registry Numbers
MDL Number MFCD28738484
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the preparation of more complex molecules, particularly in pharmaceutical research and development. Its bromine atom makes it suitable for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse chemical structures. Additionally, it finds application in the synthesis of agrochemicals and specialty chemicals, where its aromatic ester functionality contributes to the development of compounds with specific biological or physical properties. Its role in material science is also notable, particularly in the design of organic electronic materials or polymers.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,812.50
inventory 1g
10-20 days ฿4,257.00
inventory 250mg
10-20 days ฿2,124.00

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Methyl 3-bromo-2,6-dimethylbenzoate
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This compound is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the preparation of more complex molecules, particularly in pharmaceutical research and development. Its bromine atom makes it suitable for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse chemical structures. Additionally, it finds application in the synthesis of agrochemicals and specialty chemicals, where

This compound is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the preparation of more complex molecules, particularly in pharmaceutical research and development. Its bromine atom makes it suitable for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse chemical structures. Additionally, it finds application in the synthesis of agrochemicals and specialty chemicals, where its aromatic ester functionality contributes to the development of compounds with specific biological or physical properties. Its role in material science is also notable, particularly in the design of organic electronic materials or polymers.

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