(2-Bromo-5-methylthiazol-4-yl)methanol

Name: (2-Bromo-5-methylthiazol-4-yl)methanol
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CAS No. 1187836-86-7
Cat. No. CS-0153447
Purity≥97%
MDL No.MFCD20039163

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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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(2-Bromo-5-methylthiazol-4-yl)methanol|CS-0153447

Structure of 1187836-86-7

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General Information

CAS No. 1187836-86-7
Cat. No. CS-0153447
Purity ≥97%
MDL No. MFCD20039163
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₅H₆BrNOS
Molecular Weight 208.08
Synonym(s) None
SMILES CC1=C(CO)N=C(Br)S1

Description

This boronate moiety integrates readily into Suzuki-Miyaura coupling reactions, offering enhanced reactivity under mild conditions. The para-nitro group facilitates efficient cross-coupling with arylboranes, enabling rapid access to functionalized heterocycles in synthetic workflows.

Application

(2-Bromo-5-methylthiazol-4-yl)methanol serves as a versatile building block for thiazole-based heterocycles, enabling efficient functionalization via nucleophilic substitution and cross-coupling reactions. Its bromo group facilitates palladium-catalyzed transformations, while the pendant alcohol supports derivatization or protection strategies. The molecule exhibits bench stability and compatibility with standard synthetic workflows, making it suitable for medicinal chemistry campaigns and API intermediate development.

Safety Information

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GHS Pictogram :	GHS No : GHS06
Signal Word : Danger	UN#: 2811
Class : 6.1	Packing Group : Ⅲ
Hazard Statements : H301-H311-H331
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501

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Computational Chemistry Data

TPSA 33.12
LogP 1.70632
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Thiazole compounds

Key Words

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(2-Bromo-5-methylthiazol-4-yl)methanol

CAS No. 1187836-86-7

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