Methyl 2-aminopyridine-3-carboxylate
Methyl 2-aminopyridine-3-carboxylate (CAS: 14667-47-1), with the molecular formula C7H8N2O2 and a molecular weight of 152.15 g/mol, is a valuable heterocyclic building block. This compound serves as a key intermediate in organic synthesis, particularly for the construction of more complex pyridine derivatives. Its defined structure and reactivity make it a useful reagent in chemical research and development, contributing to advancements in various fields of chemical science.
- IUPAC
- Methyl 2-aminonicotinate
- Synonyms
- Methyl 2-aminonicotinate

Organic Synthesis Intermediate
Serves as a crucial building block for the synthesis of novel organic molecules, particularly nitrogen-containing heterocycles. It is employed in multi-step synthetic routes requiring pyridine ring functionalization.
Pharmaceutical Research
Utilised as a precursor in the development of potential pharmaceutical agents. The pyridine scaffold is prevalent in many biologically active compounds, making this a relevant intermediate for drug discovery programs.
Chemical Research and Development
A versatile reagent for academic and industrial R&D laboratories exploring new synthetic methodologies or creating novel chemical entities. Its availability supports diverse research projects.
| Molecular weight | 152.15 |
|---|---|
| Empirical formula | C7H8N2O2 |
| Assay | 97% |
| Melting point | 82-86 °C |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Methyl 2-aminopyridine-3-carboxylate used for?
+
Methyl 2-aminopyridine-3-carboxylate (CAS: 14667-47-1) is primarily used as an intermediate in organic synthesis, particularly for creating complex pyridine derivatives, and in pharmaceutical research and chemical development.
What are the CAS number and formula for Methyl 2-aminopyridine-3-carboxylate?
+
The CAS number is 14667-47-1, and the molecular formula is C7H8N2O2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Methyl 2-aminopyridine-3-carboxylate with a minimum assay of 97%. We do not represent this product as USP, EP, BP, or any pharmacopoeial grade.
What are the safety and handling considerations for this chemical?
+
According to the supplied safety data, this compound is classified under Water Hazard Class 2 (WGK 2) in Germany, indicating it is hazardous to aquatic life. Appropriate personal protective equipment should be used, and handling should occur in a well-ventilated area to avoid exposure.
Is Methyl 2-aminopyridine-3-carboxylate available for export?
+
Yes, Tech Serve Solutions is a global supplier and exporter of fine chemicals, including Methyl 2-aminopyridine-3-carboxylate, and can facilitate international orders.
How can I request a quote or sample?
+
To request a quote or a sample, please contact our sales department via the website or provided contact information, specifying the product CAS number (14667-47-1) and desired quantity.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis