CAS 4869-11-8

Benzenamine, 2,3-dimethyl-N-phenyl-

Description:

Benzenamine, 2,3-dimethyl-N-phenyl- is an organic compound characterized by its amine functional group attached to a benzene ring, with additional methyl groups at the 2 and 3 positions of the ring. This compound is part of the aniline family, where the nitrogen atom is bonded to a phenyl group, contributing to its aromatic properties. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. The presence of the methyl groups influences its physical and chemical properties, such as solubility and reactivity. It is generally soluble in organic solvents but has limited solubility in water due to its hydrophobic aromatic structure. This compound may be used in various applications, including as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Safety considerations should be taken into account, as it may pose health risks if inhaled or ingested, and appropriate handling procedures should be followed to minimize exposure.

Formula: C₁₄H₁₅N

Mefenamic Acid EP Impurity E

CAS: 4869-11-8

Formula: C₁₄H₁₅N

Color and Shape: Pale Yellow Solid

Molecular weight: 197.28

Ref: 4Z-M-017

2,3-Dimethyl-N-phenylbenzenamine

Controlled Product

CAS: 4869-11-8

Applications 2,3-Dimethyl-N-phenylbenzenamine is a lipophilic compound that is a commonly used non-steroidal anti-inflammatory drug (NSAID).
References El Haj, B. M., et al.: Forensic Sci. Int., 105, 141 (1999); Velkov, T., et al.: Chem. Biol., 14, 453 (2007)

Formula: C₁₄H₁₅N

Color and Shape: White To Beige

Molecular weight: 197.28

Ref: TR-D487405

2,3-Dimethyl-N-phenylbenzenamine

CAS: 4869-11-8

2,3-Dimethyl-N-phenylbenzenamine is a medicinal compound that has been found in urine and has shown potential as an anticancer agent. It acts as a kinase inhibitor, specifically targeting proteins involved in cancer cell growth and survival. In Chinese hamster ovary cells, this compound has been shown to inhibit the activity of protein kinases and induce apoptosis, or programmed cell death. This analog also displays potent antitumor activity against leukemia cells in vitro. As a promising candidate for cancer treatment, 2,3-Dimethyl-N-phenylbenzenamine may serve as a valuable tool in developing novel inhibitors for various types of cancers.

Formula: C₁₄H₁₅N

Purity: Min. 95%

Molecular weight: 197.27 g/mol

Ref: 3D-EAA86911

Mefenamic Acid EP Impurity E

CAS: 4869-11-8

Formula: C₁₄H₁₅N

Molecular weight: 197.28

Ref: ST-EA-CP-M4005