Methyl 5-bromo-6-hydroxypyridine-3-carboxylate

≥95%

Reagent Code: #205593
label
Alias 2-hydroxy-3-bromo-5-acetate pyridine; 2-hydroxy-3-bromo-pyridine-5-carboxylate methyl ester
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CAS Number 381247-99-0

science Other reagents with same CAS 381247-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.03 g/mol
Formula C₇H₆BrNO₃
badge Registry Numbers
MDL Number MFCD08235247
thermostat Physical Properties
Melting Point 225-227 °C
Boiling Point 353.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective modifications through cross-coupling reactions, nucleophilic substitutions, and ester hydrolysis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid pyridine scaffold and ease of derivatization. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and target specificity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,710.00
inventory 10g
10-20 days ฿4,580.00
inventory 25g
10-20 days ฿9,730.00
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Methyl 5-bromo-6-hydroxypyridine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective modifications through cross-coupling reactions, nucleophilic substitutions, and ester hydrolysis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid pyridine scaffol

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its functional groups—bromine, hydroxyl, and ester—allow for selective modifications through cross-coupling reactions, nucleophilic substitutions, and ester hydrolysis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid pyridine scaffold and ease of derivatization. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and target specificity.

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