CAS 21597-54-6
:Methyl 3-amino-2-naphthalenecarboxylate
Description:
Methyl 3-amino-2-naphthalenecarboxylate, with the CAS number 21597-54-6, is an organic compound characterized by its naphthalene structure, which features a carboxylate group and an amino group. This compound typically appears as a solid or crystalline substance and is known for its aromatic properties due to the presence of the naphthalene ring. The amino group contributes to its potential as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Methyl 3-amino-2-naphthalenecarboxylate may exhibit moderate solubility in organic solvents, while its solubility in water can vary depending on pH and other conditions. The compound's reactivity is influenced by the functional groups present, allowing for various chemical transformations, such as acylation or alkylation. Additionally, it may display biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance.
Formula:C12H11NO2
InChI:InChI=1S/C12H11NO2/c1-15-12(14)10-6-8-4-2-3-5-9(8)7-11(10)13/h2-7H,13H2,1H3
InChI key:InChIKey=WHMQTPBEFHEYJI-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC2=C(C=C1N)C=CC=C2
Synonyms:- Methyl 3-amino-2-naphthoate
- Methyl 2-amino-3-naphthoate
- Methyl 3-amino-2-naphthalenecarboxylate
- 2-Naphthalenecarboxylic acid, 3-amino-, methyl ester
- 2-Naphthoic acid, 3-amino-, methyl ester
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Found 3 products.
Methyl 3-aminonaphthalene-2-carboxylate
CAS:Formula:C12H11NO2Purity:98%Color and Shape:SolidMolecular weight:201.2212methyl 3-aminonaphthalene-2-carboxylate
CAS:<p>Methyl 3-aminonaphthalene-2-carboxylate, also known as 3-amino-N-(4-hydroxyphenyl)naphthalene-2-carboxamide, is a chiral molecule that has two stereogenic centers. The crystal structure of this compound is in the form of a pyridine ring with a methyl group on one side and an amine group on the other. This molecule can serve as a sensor by reacting with metal ions to form coordination complexes with chiral recognition sites. It participates in imine formation, which can be used to imprint cotton fabrics with patterns. 3-Aminonaphthalene-2-carboxylic acid (3ANAC) is an axial diastereomer of methyl 3ANAC. The signal for this compound is a pyridine ring at the top of the molecule.</p>Formula:C12H11NO2Purity:Min. 95%Molecular weight:201.2 g/mol


