(5-bromo-2-chloropyridin-3-yl)methanol

95%

Reagent Code: #150173
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CAS Number 742100-75-0

science Other reagents with same CAS 742100-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.47 g/mol
Formula C₆H₅BrClNO
badge Registry Numbers
MDL Number MFCD08688594
thermostat Physical Properties
Boiling Point 320.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its functionalized pyridine core allows for selective transformations, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions and nucleophilic substitutions to build active ingredients in crop protection agents. Also utilized in research for creating novel kinase inhibitors and other therapeutic agents due to its ability to enhance binding selectivity in molecular design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,110.00
inventory 1g
10-20 days ฿3,310.00
inventory 5g
10-20 days ฿11,910.00

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(5-bromo-2-chloropyridin-3-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its functionalized pyridine core allows for selective transformations, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions and nucleophilic substitutions to build active ingredients in crop protection agents. Also utilized in research for creating novel kinase inhibitors and other therapeutic agents due to it

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its functionalized pyridine core allows for selective transformations, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions and nucleophilic substitutions to build active ingredients in crop protection agents. Also utilized in research for creating novel kinase inhibitors and other therapeutic agents due to its ability to enhance binding selectivity in molecular design.

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