logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Oxadiazoles  > Ethyl 5-(chloromethyl)-1,2,4-oxadiazole-3-carboxylate

AA04118

1009620-97-6 | Ethyl 5-(chloromethyl)-1,2,4-oxadiazole-3-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $98.00 $69.00 -   +
1g 97% in stock $219.00 $153.00 -   +
5g 97% in stock $760.00 $532.00 -   +
10g 97% in stock $1,319.00 $923.00 -   +
25g 97% in stock $2,625.00 $1,837.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA04118
Chemical Name: Ethyl 5-(chloromethyl)-1,2,4-oxadiazole-3-carboxylate
CAS Number: 1009620-97-6
Molecular Formula: C6H7ClN2O3
Molecular Weight: 190.5844
MDL Number: MFCD11052346
SMILES: CCOC(=O)c1noc(n1)CCl

 

Computed Properties
Complexity: 167  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 4  
XLogP3: 1.1  

 

 

Upstream Synthesis Route
  • Ethyl 5-(chloromethyl)-1,2,4-oxadiazole-3-carboxylate is a versatile compound that finds application in various chemical synthesis processes. This compound serves as a key building block in the creation of diverse organic molecules due to its unique structure and reactivity. When utilized in chemical synthesis, Ethyl 5-(chloromethyl)-1,2,4-oxadiazole-3-carboxylate participates in a range of reactions such as substitution, addition, and condensation, leading to the formation of novel compounds with potential pharmaceutical, agrochemical, or material science applications. Its chloromethyl group offers a convenient handle for further functionalization, allowing for the introduction of various substituents to tailor the properties of the final product. Furthermore, the presence of the oxadiazole ring enhances the compound's stability and influences its reactivity, making it an attractive molecule for designing and accessing complex chemical structures in synthetic chemistry endeavors.
FEATURED PRODUCTS