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Home  > Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate

AA00135

1000017-97-9 | Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $58.00 $41.00 -   +
1g 96% in stock $110.00 $77.00 -   +
5g 96% in stock $463.00 $324.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA00135
Chemical Name: Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate
CAS Number: 1000017-97-9
Molecular Formula: C10H11N3O2
Molecular Weight: 205.2132
MDL Number: MFCD22989346
SMILES: CCOC(=O)c1cn2c(n1)cccc2N

 

Computed Properties
Complexity: 247  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate is a versatile compound commonly used in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the preparation of various organic molecules. In synthetic chemistry, it is frequently employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Its functional groups allow for selective modifications, making it a valuable tool for the design and creation of complex molecular structures. The presence of the amino and carboxylate groups, in particular, enables diverse chemical transformations, such as nucleophilic substitution, condensation reactions, and cyclization processes. This versatility makes Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate a crucial component in the construction of heterocyclic compounds and biologically active molecules.Furthermore, the compatibility of Ethyl 5-aminoimidazo[1,2-a]pyridine-2-carboxylate with various reagents and reaction conditions enhances its utility in synthetic applications. Its incorporation into synthetic routes allows chemists to access novel structures with precise control over regioselectivity and stereochemistry. By serving as a strategic building block, this compound facilitates the efficient and rapid synthesis of target molecules with high purity and yield.
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