CAS 20323-74-4

Ethyl 2-amino-4,5-dimethoxybenzoate

Description:

Ethyl 2-amino-4,5-dimethoxybenzoate, with the CAS number 20323-74-4, is an organic compound that belongs to the class of benzoate esters. It features a benzoic acid derivative with two methoxy groups and an amino group, which contribute to its chemical properties. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical applications. This compound typically exhibits moderate polarity due to the combination of hydrophobic aromatic and hydrophilic functional groups. Ethyl 2-amino-4,5-dimethoxybenzoate may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, owing to its functional groups. It is often studied in the context of medicinal chemistry and organic synthesis, where its structural features can be leveraged for the development of pharmaceuticals or agrochemicals. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₁H₁₅NO₄

InChI: InChI=1/C11H15NO4/c1-4-16-11(13)7-5-9(14-2)10(15-3)6-8(7)12/h5-6H,4,12H2,1-3H3

InChI key: InChIKey=SMICMEHDDWELMR-UHFFFAOYSA-N

SMILES: C(OCC)(=O)C1=CC(OC)=C(OC)C=C1N

Synonyms:

• 2-Amino-4,5-dimethoxybenzoic acid ethyl ester
• Benzoic acid, 2-amino-4,5-dimethoxy-, ethyl ester
• Ethyl 6-aminoveratrate
• Veratric acid, 6-amino-, ethyl ester
• Ethyl 2-amino-4,5-dimethoxybenzoate

Benzoic acid, 2-amino-4,5-dimethoxy-, ethyl ester

CAS: 20323-74-4

Formula: C₁₁H₁₅NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 225.2411

Ref: IN-DA0028QF

Ethyl 6-amino-3,4-dimethoxybenzoate

CAS: 20323-74-4

Ethyl 6-amino-3,4-dimethoxybenzoate

Purity: 97%

Molecular weight: 225.24g/mol

Ref: 54-OR96104

Ethyl 6-aminoveratrate

CAS: 20323-74-4

Ethyl 6-aminoveratrate (EAOV) is a urea derivative that has been shown to have analgesic effects in vitro and in vivo. EAOV was found to be more potent than morphine, but with less side effects. EAOV's antinociceptive effects are due to its ability to inhibit the activity of protein kinase C and phosphorylate the extracellular signal-regulated kinases ERK1/2. EAOV also showed metabolic stability and chemical stability, which may be due to its lack of reactive functional groups. The low potency of EAOV makes it an attractive candidate for research into the development of a new generation of painkillers.

Formula: C₁₁H₁₅NO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 225.24 g/mol

Ref: 3D-FE70274

Ethyl 6-amino-3,4-dimethoxybenzoate

CAS: 20323-74-4

Purity: 97%

Molecular weight: 225.2440033

Ref: 10-F791043