CAS 37466-90-3

Ethyl 3,4-diaminobenzoate

Description:

Ethyl 3,4-diaminobenzoate, also known as ethyl 3,4-diaminobenzoic acid, is an organic compound characterized by its amine and ester functional groups. It features a benzene ring substituted with two amino groups at the 3 and 4 positions and an ethyl ester group attached to the carboxylic acid. This compound is typically a white to off-white solid and is soluble in polar solvents due to the presence of the amino groups, which can engage in hydrogen bonding. Ethyl 3,4-diaminobenzoate is often used in organic synthesis and may serve as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. Its amino groups can participate in various chemical reactions, including acylation and alkylation, making it a versatile building block in synthetic chemistry. Additionally, the compound's properties may vary based on its purity and the specific conditions under which it is handled or stored. Safety precautions should be taken when working with this substance, as with many amines, due to potential toxicity and reactivity.

Formula: C₉H₁₂N₂O₂

InChI: InChI=1/C9H12N2O2/c1-2-13-9(12)6-3-4-7(10)8(11)5-6/h3-5H,2,10-11H2,1H3

SMILES: CCOC(=O)c1ccc(c(c1)N)N

Ethyl 3,4-Diaminobenzoate

CAS: 37466-90-3

Formula: C₉H₁₂N₂O₂

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 180.21

Ref: 3B-E0930

Ethyl 3,4-diaminobenzoate

CAS: 37466-90-3

Formula: C₉H₁₂N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 180.2038

Ref: IN-DA003Q6E

Ethyl 3,4-diaminobenzoate

CAS: 37466-90-3

Ethyl 3,4-diaminobenzoate

Formula: C₉H₁₂N₂O₂

Purity: ≥95%

Color and Shape: brown powder

Molecular weight: 180.20g/mol

Ref: 54-OR2001

Ethyl 3,4-diaminobenzoate

CAS: 37466-90-3

Formula: C₉H₁₂N₂O₂

Purity: 98%

Color and Shape: Solid, Brown powder

Molecular weight: 180.207

Ref: 10-F020165

Ethyl 3,4-diaminobenzoate

CAS: 37466-90-3

Ethyl 3,4-diaminobenzoate is a molecule that belongs to the family of aldehydes. It has been synthesized by hydrolysis of naphthalene using hydrogen chloride in the presence of ethyl acetate and water. The synthesis process was monitored by gravimetric analysis and X-ray diffraction studies. The product was purified by recrystallization from ethanol before being characterized by single-crystal X-ray diffraction. The crystal structure has revealed two different conformations for the molecule, which are related to its mesoporous nature. The compound is an inhibitor for enzymes that control glycolysis and hydrogen bond formation, such as ferroptosis.

Formula: C₉H₁₂N₂O₂

Purity: Min. 95%

Molecular weight: 180.2 g/mol

Ref: 3D-FE34287