(3-Bromo-6-methylpyridin-2-yl)methanol

Name: (3-Bromo-6-methylpyridin-2-yl)methanol
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CAS No. 1379316-16-1
Cat. No. CS-0102731
Molecule weight202.05
Purity≥97%
MDL No.MFCD16657899

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(3-Bromo-6-methylpyridin-2-yl)methanol|CS-0102731

Structure of 1379316-16-1

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General Information

CAS No. 1379316-16-1
Cat. No. CS-0102731
Purity ≥97%
MDL No. MFCD16657899
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₈BrNO
Molecular Weight 202.05
Synonym(s) (3-Bromo-6-methyl-2-pyridinyl)methanol
SMILES OCC1=NC(C)=CC=C1Br

Description

This brominated pyridyl methanol integrates a reactive alcohol group and an electrophilic bromide, enabling direct coupling in cross-coupling reactions. The methyl substituent enhances electron density at the ring, improving stability and reactivity in transition metal-catalyzed transformations.

Application

(3-Bromo-6-methylpyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring and side chain. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the benzylic alcohol offers site-specific derivatization or protection. The molecule exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis of heterocyclic scaffolds and API intermediates.

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-H319
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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Computational Chemistry Data

TPSA 33.12
LogP 1.64482
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Key Words

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(3-Bromo-6-methylpyridin-2-yl)methanol

CAS No. 1379316-16-1

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