CAS 253120-49-9

Methyl 2-amino-3-formylbenzoate

Description:

Methyl 2-amino-3-formylbenzoate, identified by its CAS number 253120-49-9, is an organic compound that features a benzoate structure with both amino and formyl functional groups. This compound typically appears as a crystalline solid and is characterized by its aromatic ring, which contributes to its stability and reactivity. The presence of the amino group (-NH2) makes it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The formyl group (-CHO) introduces reactivity that can facilitate further transformations, such as condensation reactions. Methyl 2-amino-3-formylbenzoate is soluble in polar organic solvents, which enhances its utility in synthetic organic chemistry. Its derivatives may exhibit biological activity, making it of interest in pharmaceutical research. As with many organic compounds, handling should be done with care, considering potential toxicity and reactivity. Overall, this compound serves as a versatile intermediate in the synthesis of more complex molecules in both academic and industrial settings.

Formula: C₉H₉NO₃

InChI: InChI=1S/C9H9NO3/c1-13-9(12)7-4-2-3-6(5-11)8(7)10/h2-5H,10H2,1H3

InChI key: InChIKey=HVOMOIOWMLZJCZ-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1=C(N)C(C=O)=CC=C1

Synonyms:

• 2-Amino-3-formylbenzoic acid methyl ester
• Benzoic acid, 2-amino-3-formyl-, methyl ester
• Methyl 2-amino-3-formylbenzoate

Methyl 2-amino-3-formylbenzoate

CAS: 253120-49-9

Methyl 2-amino-3-formylbenzoate

Purity: 97%

Molecular weight: 179.18g/mol

Ref: 54-OR1036371

Methyl 2-amino-3-formylbenzoate

CAS: 253120-49-9

Purity: 97%

Molecular weight: 179.1750031

Ref: 10-F758867

Methyl 2-amino-3-formylbenzoate

CAS: 253120-49-9

Methyl 2-amino-3-formylbenzoate is a cytotoxic agent that is used in vivo to produce tumors in mice. It is an isomeric cyclohexanone, which has been shown to have potent cytotoxic activity against cancer cells. Methyl 2-amino-3-formylbenzoate has been extracted from the condensations of phenylpyruvic acid and 1-indanone. This compound binds to the surface of cancer cells, which may be due to its carboxamide groups. In addition, methyl 2-amino-3-formylbenzoate has been shown to have anti-inflammatory properties and inhibit tumor cell proliferation.

Formula: C₉H₉NO₃

Purity: Min. 95%

Molecular weight: 179.17 g/mol

Ref: 3D-DKA12049