3914-42-9 | 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$14.00	$10.00
5g	98%	in stock	$69.00	$49.00
10g	98%	in stock	$138.00	$97.00
25g	98%	in stock	$344.00	$241.00

Description

• Catalog Number: AB43486
• Chemical Name: 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole
• CAS Number: 3914-42-9
• Molecular Formula: C4H5ClN2O
• Molecular Weight: 132.5483
• MDL Number: MFCD06655111
• SMILES: Cc1nnc(o1)CCl

Computed Properties

• Complexity: 80.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 0.6

Upstream Synthesis Route

The compound 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole serves as a versatile building block in chemical synthesis due to its unique reactivity and functional group compatibility. This compound is commonly employed as a precursor in the preparation of various biologically active molecules, pharmaceutical compounds, and agrochemicals.One significant application of 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole is in the synthesis of heterocyclic compounds with diverse biological activities. By incorporating this compound into the molecular structure, chemists can introduce chloromethyl and methyl groups at specific positions, enabling the modification of pharmacological properties such as bioavailability, potency, and selectivity. Moreover, the oxadiazole ring system can impart desirable properties to the final products, making it a valuable scaffold in drug discovery and development.Furthermore, the chloromethyl group in 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole can undergo various chemical transformations such as nucleophilic substitution and cross-coupling reactions. This reactivity enables the incorporation of the oxadiazole moiety into more complex molecular frameworks, allowing for the synthesis of structurally diverse compounds with tailored properties.Overall, the strategic use of 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole in chemical synthesis provides synthetic chemists with a powerful tool for the construction of novel molecules with potential applications in the fields of medicine, agriculture, and materials science.