Cas no 179555-12-5 (methyl 6-amino-4-methyl-pyridine-3-carboxylate)

Methyl 6-amino-4-methyl-pyridine-3-carboxylate is a versatile pyridine derivative with applications in pharmaceutical and agrochemical synthesis. Its structure, featuring both an amino and ester functional group, makes it a valuable intermediate for constructing heterocyclic compounds. The methyl ester moiety enhances solubility in organic solvents, facilitating further derivatization, while the amino group provides a reactive site for coupling reactions. This compound is particularly useful in medicinal chemistry for developing bioactive molecules due to its stable pyridine core and modifiable functional groups. High purity grades are available, ensuring consistency in research and industrial processes. Proper handling under controlled conditions is recommended due to its sensitivity to moisture and heat.
methyl 6-amino-4-methyl-pyridine-3-carboxylate structure
179555-12-5 structure
Product Name:methyl 6-amino-4-methyl-pyridine-3-carboxylate
CAS No:179555-12-5
MF:C8H10N2O2
MW:166.177201747894
MDL:MFCD18803290
CID:1107948
PubChem ID:9877474
Update Time:2025-10-05

methyl 6-amino-4-methyl-pyridine-3-carboxylate Chemical and Physical Properties

Names and Identifiers

    • 6-amino-4-methyl-3-Pyridinecarboxylic acid methyl ester
    • methyl 6-amino-4-methylnicotinate
    • methyl 6-amino-4-methyl-pyridine-3-carboxylate
    • 6-Amino-4-methyl-nicotinic acid methyl ester
    • SCHEMBL2012842
    • 6-Amino-4-methylnicotinic acid methyl ester
    • A934613
    • DB-334710
    • AKOS027321754
    • PRFJNCHHLJFFSN-UHFFFAOYSA-N
    • CS-0242014
    • MFCD18803290
    • SB53602
    • 179555-12-5
    • F83182
    • Methyl6-amino-4-methylnicotinate
    • EN300-243305
    • 2-Amino-5-methoxycarbonyl-4-methylpyridine
    • METHYL 6-AMINO-4-METHYLPYRIDINE-3-CARBOXYLATE
    • Z1216823926
    • MDL: MFCD18803290
    • Inchi: 1S/C8H10N2O2/c1-5-3-7(9)10-4-6(5)8(11)12-2/h3-4H,1-2H3,(H2,9,10)
    • InChI Key: PRFJNCHHLJFFSN-UHFFFAOYSA-N
    • SMILES: O(C)C(C1=CN=C(C=C1C)N)=O

Computed Properties

  • Exact Mass: 166.0743
  • Monoisotopic Mass: 166.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 172
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.7
  • Topological Polar Surface Area: 65.2?2

Experimental Properties

  • PSA: 65.21

methyl 6-amino-4-methyl-pyridine-3-carboxylate Pricemore >>

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Additional information on methyl 6-amino-4-methyl-pyridine-3-carboxylate

Comprehensive Overview of Methyl 6-Amino-4-methyl-pyridine-3-carboxylate (CAS No. 179555-12-5)

Methyl 6-amino-4-methyl-pyridine-3-carboxylate (CAS No. 179555-12-5) is a specialized organic compound widely recognized for its versatile applications in pharmaceutical research, agrochemical development, and material science. This pyridine derivative, characterized by its amino and ester functional groups, has garnered significant attention due to its role as a key intermediate in synthesizing bioactive molecules. Its molecular structure, C8H10N2O2, offers unique reactivity, making it valuable for heterocyclic chemistry and drug discovery.

In recent years, the demand for methyl 6-amino-4-methyl-pyridine-3-carboxylate has surged, driven by its utility in designing kinase inhibitors and antimicrobial agents. Researchers highlight its potential in addressing antibiotic resistance, a pressing global health challenge. The compound’s pyridine core is instrumental in modulating electronic properties, which aligns with trends in green chemistry and sustainable synthesis. These attributes make it a focal point for innovations in catalysis and bioconjugation techniques.

The synthesis of CAS No. 179555-12-5 typically involves multistep organic reactions, including esterification and amination, with yields optimized through modern microwave-assisted synthesis. Analytical techniques like HPLC and NMR ensure high purity, critical for its use in high-throughput screening (HTS) platforms. Notably, its stability under ambient conditions enhances its practicality for industrial-scale applications, such as crop protection formulations and electronic materials.

From an SEO perspective, queries like "pyridine derivatives in drug design", "applications of methyl 6-amino-4-methyl-pyridine-3-carboxylate", and "CAS 179555-12-5 supplier" reflect growing interest. Addressing these, this compound’s compatibility with click chemistry and metal-organic frameworks (MOFs) positions it at the forefront of interdisciplinary research. Its low environmental persistence, as per REACH compliance, further boosts its adoption in eco-friendly applications.

Future prospects for methyl 6-amino-4-methyl-pyridine-3-carboxylate include explorations in neurodegenerative disease therapeutics and photovoltaic materials. Collaborative studies between academia and industry aim to unlock its full potential, reinforcing its status as a high-value chemical building block. As regulatory frameworks evolve, its non-hazardous profile ensures sustained relevance in global markets.

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