methyl 3-amino-6-methylpyrazine-2-carboxylate
$600.00
CAS No.: 2032-84-0
Catalog No.: 192862
Purity: 95%
MF: C7H9N3O2
MW: 167.168
Storage: 2-8 degree Celsius
SMILES: NC=1C(=NC(=CN1)C)C(=O)OC
Catalog No.: 192862
Purity: 95%
MF: C7H9N3O2
MW: 167.168
Storage: 2-8 degree Celsius
SMILES: NC=1C(=NC(=CN1)C)C(=O)OC
methyl 3-amino-6-methylpyrazine-2-carboxylate; CAS No.: 2032-84-0; methyl 3-amino-6-methylpyrazine-2-carboxylate. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C7H8N2O2 and a molecular weight of 152.15 g/mol. It exhibits a melting point in the range of 98-102 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to acidic conditions and should be stored in neutral to slightly basic environments. Recommended storage conditions include tightly sealed containers at temperatures below 30 C, protected from light and moisture. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as methyl 3-amino-6-methylpyrazine-2-carboxylate may cause mild skin and eye irritation upon contact. The amine functionality requires careful handling in oxidative environments. APPLICATIONS: As a key intermediate in the synthesis of veterinary pharmaceuticals, methyl 3-amino-6-methylpyrazine-2-carboxylate has been utilized in the preparation of antiparasitic agents, as documented in veterinary medicinal chemistry publications. Its amino group enables further functionalization for developing antimicrobial compounds. Additionally, this compound serves as a building block for preparing agricultural fungicides through substitution reactions at the amino position. Academic research has explored its potential in click chemistry reactions for creating bioactive molecules, as reported in organic chemistry journals. The methyl substituent also facilitates improved solubility profiles in organic media, making it valuable for preparing pyrazine-based liquid crystalline materials in materials science, as evidenced by studies in polymer chemistry literature.
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