3-Bromo-5-pyridinemethanol

98%

Reagent Code: #143655
label
Alias 5-Bromo-3-pyridinol; 3-Bromo-5-(hydroxymethyl)pyridine
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CAS Number 37669-64-0

science Other reagents with same CAS 37669-64-0

blur_circular Chemical Specifications

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Weight 188.02 g/mol
Formula C₆H₆BrNO
badge Registry Numbers
MDL Number MFCD03265757
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and central nervous system agents. Its functional groups allow for selective derivatization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Also employed in the preparation of agrochemicals and bioactive molecules where pyridine-based scaffolds are required. Its bromine moiety facilitates cross-coupling reactions, enabling efficient construction of C–C bonds in advanced synthetic pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿156.00
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿3,006.00

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3-Bromo-5-pyridinemethanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and central nervous system agents. Its functional groups allow for selective derivatization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Also employed in the preparation of agrochemicals and bioactive molecules where pyridine-based scaffolds are required. Its bromine moiety facilitates cross-coupling reactions, enabling efficient c

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and central nervous system agents. Its functional groups allow for selective derivatization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Also employed in the preparation of agrochemicals and bioactive molecules where pyridine-based scaffolds are required. Its bromine moiety facilitates cross-coupling reactions, enabling efficient construction of C–C bonds in advanced synthetic pathways.

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