Methyl 6-bromo-3-hydroxy-2-methylbenzoate

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Reagent Code: #203360
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CAS Number 55289-15-1

science Other reagents with same CAS 55289-15-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.0742 g/mol
Formula C₉H₉BrO₃
badge Registry Numbers
MDL Number MFCD16660005
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective chemical modifications, enabling coupling reactions, cyclizations, and derivatizations in multi-step organic syntheses. Commonly employed in research settings to construct complex benzene derivatives with tailored biological activity. Also utilized in the preparation of agrochemicals and specialty polymers due to its structural stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,580.00
inventory 1g
10-20 days ฿25,580.00
inventory 250mg
10-20 days ฿9,470.00

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Methyl 6-bromo-3-hydroxy-2-methylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective chemical modifications, enabling coupling reactions, cyclizations, and derivatizations in multi-step organic syntheses. Commonly employed in research settings to construct complex benzene derivatives with tailored biological activity. Also utilized in the prepar

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective chemical modifications, enabling coupling reactions, cyclizations, and derivatizations in multi-step organic syntheses. Commonly employed in research settings to construct complex benzene derivatives with tailored biological activity. Also utilized in the preparation of agrochemicals and specialty polymers due to its structural stability and reactivity profile.

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