Methyl 3-bromo-2-hydroxybenzoate

98%

Reagent Code: #207292
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CAS Number 28165-45-9

science Other reagents with same CAS 28165-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.04 g/mol
Formula C₈H₇BrO₃
badge Registry Numbers
MDL Number MFCD10566798
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, hydroxyl, and ester—allow for selective reactions such as cross-coupling, ester hydrolysis, or ether formation. Commonly employed in the development of bioactive molecules where substituted benzoate scaffolds are required. Also utilized in research settings for constructing complex aromatic compounds through nucleophilic substitution or metal-catalyzed transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿540.00
1g
10-20 days ฿1,130.00
5g
10-20 days ฿3,820.00
25g
10-20 days ฿17,670.00
100g
10-20 days ฿65,400.00
Methyl 3-bromo-2-hydroxybenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, hydroxyl, and ester—allow for selective reactions such as cross-coupling, ester hydrolysis, or ether formation. Commonly employed in the development of bioactive molecules where substituted benzoate scaffolds are required. Also utilized in research settings for constructing complex aromatic compounds through nucleophilic substitution or metal-catalyzed transfo

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, hydroxyl, and ester—allow for selective reactions such as cross-coupling, ester hydrolysis, or ether formation. Commonly employed in the development of bioactive molecules where substituted benzoate scaffolds are required. Also utilized in research settings for constructing complex aromatic compounds through nucleophilic substitution or metal-catalyzed transformations.

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