5-Bromopyridine-3-sulfonic acid

95%

Reagent Code: #150765
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CAS Number 62009-34-1

science Other reagents with same CAS 62009-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.06 g/mol
Formula C₅H₄BrNO₃S
badge Registry Numbers
MDL Number MFCD00717696
thermostat Physical Properties
Melting Point >300 °C
inventory_2 Storage & Handling
Density 1.957±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. Its bromine and sulfonic acid functional groups allow for selective cross-coupling reactions and sulfonation modifications, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing kinase inhibitors and nicotinic acetylcholine receptor ligands. Also utilized in materials science for designing functionalized polymers and catalysts due to its ability to coordinate with metal centers.

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Test Parameter Specification
Appearance Light yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,010.00
inventory 5g
10-20 days ฿14,640.00
inventory 25g
10-20 days ฿39,600.00

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5-Bromopyridine-3-sulfonic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. Its bromine and sulfonic acid functional groups allow for selective cross-coupling reactions and sulfonation modifications, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing kinase inhibitors and nicotinic acetylcholine receptor ligands. Also utilized in materials science for designing function

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. Its bromine and sulfonic acid functional groups allow for selective cross-coupling reactions and sulfonation modifications, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing kinase inhibitors and nicotinic acetylcholine receptor ligands. Also utilized in materials science for designing functionalized polymers and catalysts due to its ability to coordinate with metal centers.

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