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

Name: (5-Methyl-1,3,4-thiadiazol-2-yl)methanol
Brand: ChemScene
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CAS No. 869108-51-0
Cat. No. CS-0187970
Purity≥97%
MDL No.None

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(5-Methyl-1,3,4-thiadiazol-2-yl)methanol|CS-0187970

Structure of 869108-51-0

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Description

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol features a methyl-substituted thiadiazole ring linked to a primary alcohol group, delivering enhanced solubility and reactivity. This scaffold integrates readily into heterocyclic synthesis, serving as a versatile synthon for medicinal chemistry and materials science applications.

Application

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through its reactive methylene group. The molecule exhibits bench stability and tolerates common functional groups, facilitating straightforward incorporation into diverse scaffolds via nucleophilic substitution or coupling reactions. Its well-defined reactivity profile supports efficient synthesis of potential drug candidates and functionalized intermediates in standard organic workflows.

General Information

CAS No. 869108-51-0
Cat. No. CS-0187970
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₄H₆N₂OS
Molecular Weight 130.17
Synonym(s) None
SMILES CC1=NN=C(CO)S1

Computational Chemistry Data

TPSA 46.01
LogP 0.33882
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 1

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
Precautionary Statements : P264-P270-P330-P501

Quality Control

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Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Thiadiazole compounds

Key Words

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

CAS No. 869108-51-0

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