CAS 60075-23-2

3,4-Dimethoxyphenylacetic acid hydrazide

Description:

3,4-Dimethoxyphenylacetic acid hydrazide is an organic compound characterized by the presence of a hydrazide functional group attached to a phenylacetic acid moiety that features two methoxy groups at the 3 and 4 positions of the aromatic ring. This compound typically appears as a white to off-white solid and is soluble in organic solvents, with limited solubility in water due to its hydrophobic aromatic structure. The presence of the hydrazide group suggests potential reactivity, particularly in forming hydrazones or undergoing condensation reactions. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of anti-inflammatory or antimicrobial agents. The compound's molecular structure contributes to its chemical properties, influencing its reactivity, stability, and interaction with biological systems. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity or reactivity.

Formula: C₁₀H₁₄N₂O₃

InChI: InChI=1/C10H14N2O3/c1-14-8-4-3-7(5-9(8)15-2)6-10(13)12-11/h3-5H,6,11H2,1-2H3,(H,12,13)

SMILES: COc1ccc(cc1OC)CC(=NN)O

Synonyms:

• 3,4-Dimethoxyphenylacethydrazide~Homoveratric acid hydrazide
• 2-(3,4-Dimethoxyphenyl)Acetohydrazide

3,4-Dimethoxyphenylacetic acid hydrazide

CAS: 60075-23-2

Formula: C₁₀H₁₄N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 210.2298

Ref: IN-DA003IIC

3,4-Dimethoxyphenylacetic acid hydrazide

CAS: 60075-23-2

3,4-Dimethoxyphenylacetic acid hydrazide

Purity: 98%

Color and Shape: Solid

Molecular weight: 210.23g/mol

Ref: 54-OR0165

3,4-Dimethoxyphenylacetic acid hydrazide

CAS: 60075-23-2

Formula: C₁₀H₁₄N₂O₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 210.233

Ref: 10-F011157

2-(3,4-Dimethoxyphenyl)acetohydrazide

CAS: 60075-23-2

2-(3,4-Dimethoxyphenyl)acetohydrazide (2DMAH) is an alpha-amylase inhibitor that is used to treat type 2 diabetes. It has been shown to inhibit the activity of α-amylase in human pancreatic juice and serum. 2DMAH has a number of phenyl groups that are responsible for its inhibition of carbohydrate metabolism. The crystal x-ray diffraction profile of 2DMAH shows a single peak at around 5.5° angle, which is characteristic of phenyl rings. When 2DMAH is dissolved in sodium hydroxide solution, it modulates the neurotoxicity induced by methamphetamine and other amphetamine derivatives. This compound also inhibits the production of collagen and thiosemicarbazide, which may be beneficial for the treatment of cancerous tumors.

Formula: C₁₀H₁₄N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 210.23 g/mol

Ref: 3D-FD112855