Methyl 4-bromo-3,5-dihydroxybenzoate

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Reagent Code: #47424
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CAS Number 34126-16-4

science Other reagents with same CAS 34126-16-4

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Weight 247.0400 g/mol
Formula C₈H₇BrO₄
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MDL Number MFCD03840476
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Methyl 4-bromo-3,5-dihydroxybenzoate is primarily used in organic synthesis as an intermediate for the production of more complex chemical compounds. Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom in the molecule allows for further functionalization through various coupling reactions, such as Suzuki or Heck reactions, which are essential in creating biologically active molecules. Additionally, its phenolic hydroxyl groups can be modified to form ethers or esters, expanding its utility in the development of polymers and coatings. This compound is particularly valuable in medicinal chemistry for designing drug candidates with specific biological activities.

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inventory 250mg
10-20 days ฿2,871.00

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Methyl 4-bromo-3,5-dihydroxybenzoate
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Methyl 4-bromo-3,5-dihydroxybenzoate is primarily used in organic synthesis as an intermediate for the production of more complex chemical compounds. Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom in the molecule allows for further functionalization through various coupling reactions, such as Suzuki or Heck reactions, which are essential in creating biolog

Methyl 4-bromo-3,5-dihydroxybenzoate is primarily used in organic synthesis as an intermediate for the production of more complex chemical compounds. Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom in the molecule allows for further functionalization through various coupling reactions, such as Suzuki or Heck reactions, which are essential in creating biologically active molecules. Additionally, its phenolic hydroxyl groups can be modified to form ethers or esters, expanding its utility in the development of polymers and coatings. This compound is particularly valuable in medicinal chemistry for designing drug candidates with specific biological activities.

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