(4-Bromopyridin-2-yl)methanol

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Reagent Code: #145203
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CAS Number 131747-45-0

science Other reagents with same CAS 131747-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.02 g/mol
Formula C₆H₆BrNO
thermostat Physical Properties
Boiling Point 284.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the pyridyl moiety into target molecules. Also utilized in agrochemical research for designing new active ingredients. The hydroxyl and bromo groups provide dual reactivity, enabling sequential transformations in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿840.00
inventory 5g
10-20 days ฿2,900.00
inventory 25g
10-20 days ฿11,620.00

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(4-Bromopyridin-2-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the pyridyl moiety into target molecules. Also utilized in agrochemical research for designing new active ingredients.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the pyridyl moiety into target molecules. Also utilized in agrochemical research for designing new active ingredients. The hydroxyl and bromo groups provide dual reactivity, enabling sequential transformations in multi-step organic syntheses.

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