Methyl 5-bromo-2-hydroxy-3-methoxybenzoate

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Reagent Code: #207272
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CAS Number 134419-43-5

science Other reagents with same CAS 134419-43-5

blur_circular Chemical Specifications

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Weight 261.07 g/mol
Formula C₉H₉BrO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its functional groups—bromine, hydroxyl, and methoxy—allow for selective reactions such as cross-coupling, etherification, and ester modifications. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory or antimicrobial agents. The bromine atom facilitates metal-catalyzed coupling reactions, enabling the construction of complex aromatic structures. Also utilized in research settings for the synthesis of natural product analogs and drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿4,600.00
inventory 5g
10-20 days ฿12,900.00

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Methyl 5-bromo-2-hydroxy-3-methoxybenzoate
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its functional groups—bromine, hydroxyl, and methoxy—allow for selective reactions such as cross-coupling, etherification, and ester modifications. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory or antimicrobial agents. The bromine atom facilitates metal-catalyzed coupling reactions, enabling the construction of complex aromatic structures. Also utilized in research set

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its functional groups—bromine, hydroxyl, and methoxy—allow for selective reactions such as cross-coupling, etherification, and ester modifications. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory or antimicrobial agents. The bromine atom facilitates metal-catalyzed coupling reactions, enabling the construction of complex aromatic structures. Also utilized in research settings for the synthesis of natural product analogs and drug candidates.

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