(5-Bromo-1,3,4-thiadiazol-2-yl)methanol

Name: (5-Bromo-1,3,4-thiadiazol-2-yl)methanol
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CAS No. 1339055-00-3
Cat. No. CS-0132211
Purity≥95%
MDL No.None

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Type	HazMat Fee
Excepted Quantity	$0.00
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(5-Bromo-1,3,4-thiadiazol-2-yl)methanol|CS-0132211

Structure of 1339055-00-3

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Description

This bench-stable, moisture-tolerant reagent features a brominated thiadiazole ring fused with a hydroxymethyl group, enabling direct incorporation into bioconjugation workflows. The electrophilic bromine site facilitates selective coupling reactions under mild conditions, while the polar alcohol moiety enhances solubility in aqueous and organic media.

Application

(5-Bromo-1,3,4-thiadiazol-2-yl)methanol serves as a versatile building block for constructing bioactive heterocycles, enabling direct functionalization at the thiadiazole core. Its bromine and hydroxymethyl groups offer orthogonal reactivity for cross-coupling, derivatization, and protection strategies. The compound exhibits bench stability and facilitates efficient purification, making it suitable for iterative synthesis in medicinal chemistry and process development workflows.

General Information

CAS No. 1339055-00-3
Cat. No. CS-0132211
Purity ≥95%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₃H₃BrN₂OS
Molecular Weight 195.04
Synonym(s) 1,3,4-Thiadiazole-2-Methanol, 5-broMo-
SMILES OCC1=NN=C(Br)S1

Computational Chemistry Data

TPSA 46.01
LogP 0.7929
H_Acceptors 4
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-P330-P362+P364-P405-P501

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Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Thiadiazole compounds

Key Words

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(5-Bromo-1,3,4-thiadiazol-2-yl)methanol

CAS No. 1339055-00-3

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