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Home  > Ethyl 4-amino-2-chloropyrimidine-5-carboxylate

AB48301

71406-78-5 | Ethyl 4-amino-2-chloropyrimidine-5-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $13.00 $9.00 -   +
250mg 97% in stock $16.00 $11.00 -   +
1g 97% in stock $35.00 $24.00 -   +
5g 97% in stock $148.00 $103.00 -   +
10g 97% in stock $279.00 $196.00 -   +
25g 97% in stock $560.00 $392.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB48301
Chemical Name: Ethyl 4-amino-2-chloropyrimidine-5-carboxylate
CAS Number: 71406-78-5
Molecular Formula: C7H8ClN3O2
Molecular Weight: 201.6103
MDL Number: MFCD09860847
SMILES: CCOC(=O)c1cnc(nc1N)Cl

 

Upstream Synthesis Route
  • Ethyl 4-amino-2-chloropyrimidine-5-carboxylate is a versatile compound widely utilized in chemical synthesis for its ability to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. This compound plays a crucial role in the development of innovative drug molecules due to its unique structural properties and reactivity in organic reactions.In chemical synthesis, Ethyl 4-amino-2-chloropyrimidine-5-carboxylate can undergo various transformations such as substitution, addition, and condensation reactions to introduce different functional groups at specific positions on the pyrimidine ring. This flexibility enables chemists to tailor the molecular structure of target compounds, modulate their physicochemical properties, and enhance their biological activities.Furthermore, the presence of both an amino group and a carboxylate group in Ethyl 4-amino-2-chloropyrimidine-5-carboxylate provides opportunities for further derivatization and molecular diversification. These functional groups can participate in key synthetic steps like amide bond formation, esterification, and salt formation, allowing for the creation of complex molecules with specific properties and functions.Overall, the strategic use of Ethyl 4-amino-2-chloropyrimidine-5-carboxylate in chemical synthesis enables the efficient construction of structurally diverse and biologically active compounds, making it a valuable tool in the development of new drugs, agrochemicals, and advanced materials.
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