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AC25938

849805-25-0 | Methyl 2-amino-6-chloronicotinate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $6.00 $5.00 -   +
250mg 98% in stock $10.00 $7.00 -   +
1g 98% in stock $27.00 $19.00 -   +
5g 98% in stock $113.00 $80.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AC25938
Chemical Name: Methyl 2-amino-6-chloronicotinate
CAS Number: 849805-25-0
Molecular Formula: C7H7ClN2O2
Molecular Weight: 186.5957
MDL Number: MFCD17015967
SMILES: COC(=O)c1ccc(nc1N)Cl

 

Computed Properties
Complexity: 177  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • Methyl 2-amino-6-chloronicotinate is a key compound in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound is commonly used as a versatile building block due to its unique structure and reactivity. In chemical synthesis, Methyl 2-amino-6-chloronicotinate acts as a valuable precursor in the creation of various biologically active molecules. Its functional groups allow for facile transformation into a range of derivatives through simple chemical reactions. This enables the synthesis of complex molecules with specific pharmaceutical or agricultural properties.The presence of an amino group and a chloro group in Methyl 2-amino-6-chloronicotinate provides opportunities for selective functionalization, leading to the introduction of diverse molecular functionalities. These functional groups can undergo various transformations such as cross-coupling reactions, nucleophilic substitutions, and cyclization reactions, allowing for the construction of structurally diverse compounds.Furthermore, Methyl 2-amino-6-chloronicotinate can participate in the formation of heterocyclic structures, which are prevalent in many biologically active compounds. By incorporating this compound into a synthetic route, chemists can access a wide range of heterocyclic scaffolds, including pyridines and pyrimidines, which are essential in drug discovery and development.Overall, the application of Methyl 2-amino-6-chloronicotinate in chemical synthesis offers a powerful tool for the efficient construction of complex molecules with potential pharmacological or agricultural significance. Its versatility and reactivity make it a valuable building block for the creation of new therapeutic agents and agrochemicals.
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