(4-Bromopyridin-3-yl)methanol

Name: (4-Bromopyridin-3-yl)methanol
Brand: ChemScene
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CAS No. 197007-87-7
Cat. No. CS-W021100
Purity≥97%
MDL No.None

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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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(4-Bromopyridin-3-yl)methanol|CS-W021100

Structure of 197007-87-7

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Description

(4-Bromopyridin-3-yl)methanol features a brominated pyridine ring bearing a reactive hydroxymethyl group, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable reagent integrates readily into complex molecular architectures, particularly in medicinal chemistry and materials synthesis.

Application

(4-Bromopyridin-3-yl)methanol serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to pyridine-based scaffolds. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the alcohol functionality offers straightforward derivatization via oxidation or protection. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical reagent for constructing functionalized heterocycles and advanced intermediates in API development.

General Information

CAS No. 197007-87-7
Cat. No. CS-W021100
Purity ≥97%
MDL No. None
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₆H₆BrNO
Molecular Weight 188.02
Synonym(s) 4-Bromo-3-pyridinemethanol
SMILES OCC1=C(Br)C=CN=C1

Computational Chemistry Data

TPSA 33.12
LogP 1.3364
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 1

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Key Words

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(4-Bromopyridin-3-yl)methanol

CAS No. 197007-87-7

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