(2-Bromothiazol-4-yl)methanol

Name: (2-Bromothiazol-4-yl)methanol
Brand: ChemScene
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CAS No. 5198-86-7
Cat. No. CS-W009239
Purity≥95%
MDL No.MFCD04115727

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(2-Bromothiazol-4-yl)methanol|CS-W009239

Structure of 5198-86-7

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Description

(2-Bromothiazol-4-yl)methanol features a brominated thiazole ring bearing a reactive hydroxymethyl group, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring heterocyclic building blocks with orthogonal reactivity.

Application

(2-Bromothiazol-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the thiazole C4 position. Its bromine moiety facilitates palladium-catalyzed cross-coupling reactions, while the alcohol group offers orthogonal reactivity for derivatization or protection. The compound exhibits good bench stability and is compatible with standard purification methods, making it suitable for iterative synthesis of heterocyclic scaffolds and API intermediates.

General Information

CAS No. 5198-86-7
Cat. No. CS-W009239
Purity ≥95%
MDL No. MFCD04115727
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₄H₄BrNOS
Molecular Weight 194.05
Synonym(s) 2-BROMO-4-HYDROXYMETHYLTHIAZOLE
SMILES OCC1=CSC(Br)=N1

Computational Chemistry Data

TPSA 33.12
LogP 1.3979
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

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-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 Thiazole compounds

Key Words

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(2-Bromothiazol-4-yl)methanol

CAS No. 5198-86-7

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