(S)-3-Bromo-2-(1-methoxyethyl)pyridine

CAS No. 2641451-44-5
Cat. No. CS-0312114
Purity≥97%
MDL No.None

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(S)-3-Bromo-2-(1-methoxyethyl)pyridine|CS-0312114

Structure of 2641451-44-5

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Description

This chiral pyridine derivative features a stereodefined bromide at the 3-position and a methoxyethyl side chain at the 2-position, enabling precise coupling in asymmetric synthesis. The bench-stable, moisture-tolerant structure facilitates efficient transition metal-catalyzed transformations and serves as a key scaffold for bioactive molecule construction.

Application

(S)-3-Bromo-2-(1-methoxyethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined stereochemistry and stable bromopyridine functionality. The methoxyethyl side chain offers moderate steric bulk and enhanced solubility, facilitating purification and downstream derivatization. This compound functions effectively in Suzuki-Miyaura and Negishi coupling protocols, providing access to complex pyridyl scaffolds relevant to pharmaceutical development.

General Information

CAS No. 2641451-44-5
Cat. No. CS-0312114
Purity ≥97%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₁₀BrNO
Molecular Weight 216.08
Synonym(s) None
SMILES C[C@@H](C1=NC=CC=C1Br)OC

Computational Chemistry Data

TPSA 22.12
LogP 2.5515
H_Acceptors 2
H_Donors 0
Rotatable_Bonds 2

Safety Information

Download SDS

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-P330-P362-P405-P501

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Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Drug Discovery Cancer KRAS

Key Words

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(S)-3-Bromo-2-(1-methoxyethyl)pyridine

CAS No. 2641451-44-5

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