AC25938
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.
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 |
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 |
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.