(2-Bromooxazol-4-yl)methanol

Name: (2-Bromooxazol-4-yl)methanol
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CAS No. 1092351-92-2
Cat. No. CS-0132194
Purity≥97%
MDL No.MFCD11109413

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General Information

CAS No. 1092351-92-2
Cat. No. CS-0132194
Purity ≥97%
MDL No. MFCD11109413
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₄H₄BrNO₂
Molecular Weight 177.98
Synonym(s) 2-Bromo-4-hydroxymethyloxazole
SMILES OCC1=COC(Br)=N1

Description

(2-Bromooxazol-4-yl)methanol features a brominated oxazolyl ring coupled to a reactive methanol handle, enabling direct functionalization in synthetic transformations. This bench-stable heterocycle integrates readily into pharmaceutical intermediates and agrochemical scaffolds, offering high regioselectivity in coupling reactions.

Application

(2-Bromooxazol-4-yl)methanol serves as a versatile building block for oxazole-based scaffolds, enabling efficient functionalization via nucleophilic substitution and cross-coupling reactions. Its bromine moiety facilitates Pd-catalyzed transformations, while the pendant alcohol group allows for derivatization or protection, offering orthogonal reactivity in complex molecule synthesis. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for medicinal chemistry and process development workflows.

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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Computational Chemistry Data

TPSA 46.26
LogP 0.9294
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Oxazole compounds

Key Words

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(2-Bromooxazol-4-yl)methanol

CAS No. 1092351-92-2

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