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

Name: (5-Methyl-1,3,4-oxadiazol-2-yl)methanol
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CAS No. 915924-37-7
Cat. No. CS-0128619
Purity≥98%
MDL No.MFCD08059900

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(5-Methyl-1,3,4-oxadiazol-2-yl)methanol|CS-0128619

Structure of 915924-37-7

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General Information

CAS No. 915924-37-7
Cat. No. CS-0128619
Purity ≥98%
MDL No. MFCD08059900
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₄H₆N₂O₂
Molecular Weight 114.10
Synonym(s) None
SMILES CC1=NN=C(CO)O1

Description

This bench-stable oxadiazole derivative features a methyl-substituted heterocyclic core paired with a reactive hydroxymethyl group. The electron-deficient 1,3,4-oxadiazole ring enhances stability while the terminal alcohol enables straightforward derivatization. This compound serves as a versatile synthetic handle for incorporating bioactive motifs into pharmaceutical and agrochemical scaffolds.

Application

(5-Methyl-1,3,4-oxadiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the efficient construction of oxadiazole-containing scaffolds. Its hydroxymethyl group facilitates downstream functionalization through etherification, esterification, or oxidation to aldehyde. The molecule exhibits good bench stability and compatibility with standard reaction conditions, making it well-suited for modular synthesis workflows targeting bioactive heterocycles.

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 : H225
Precautionary Statements : P210-P243-P273-P403

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Computational Chemistry Data

TPSA 59.15
LogP -0.12968
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Oxadiazole compounds

Key Words

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

CAS No. 915924-37-7

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