CAS 16777-78-9

Benzoic acid,4-[(phenylamino)carbonyl]-

Description:

Benzoic acid, 4-[(phenylamino)carbonyl]- is an organic compound characterized by its structure, which includes a benzoic acid moiety and a phenylamino group. This compound features a carboxylic acid functional group (-COOH) attached to a benzene ring, along with an amide linkage that connects a phenyl group to the carbonyl carbon. It is typically a white to off-white solid at room temperature and is soluble in organic solvents, but its solubility in water is limited due to the hydrophobic nature of the aromatic rings. The presence of the amine group can impart basic properties, while the carboxylic acid contributes acidic characteristics. This compound may exhibit biological activity, making it of interest in pharmaceutical and biochemical research. Its CAS number, 16777-78-9, allows for easy identification in chemical databases. As with many organic compounds, it is important to handle it with care, considering potential hazards associated with its chemical structure and reactivity.

Formula: C₁₄H₁₁NO₃

Synonyms:

• Terephthalanilicacid (8CI)
• Am 00

4-(Phenylcarbamoyl)benzoic acid

CAS: 16777-78-9

Formula: C₁₄H₁₁NO₃

Purity: 98%

Molecular weight: 241.2420

Ref: IN-DA00AQJO

4-(Phenylcarbamoyl)benzoic acid

CAS: 16777-78-9

4-(Phenylcarbamoyl)benzoic acid

Purity: 98%

Ref: 54-OR1037488

4-(Phenylcarbamoyl)benzoic acid

CAS: 16777-78-9

Purity: 98%

Molecular weight: 241.2460022

Ref: 10-F638035

4-(Phenylcarbamoyl)benzoic Acid

CAS: 16777-78-9

4-(Phenylcarbamoyl)benzoic acid is a metabolite of all-trans-retinoic acid that has been shown to induce promyelocytic leukemia in human cells. It binds to cellular retinobenzoic acid receptors, which are proteins that regulate cellular differentiation and apoptosis. The binding of 4-(phenylcarbamoyl)benzoic acid to these receptors leads to the inhibition of cellular proliferation and the induction of apoptosis in promyelocytic leukemia cells. 4-(Phenylcarbamoyl)benzoic Acid also inhibits the metabolism of retinoids by inhibiting the enzyme retinol dehydrogenase, thereby increasing the levels of all-trans-retinoic acid. This leads to an increased activity of retinoic acid on its receptor.

Formula: C₁₄H₁₁NO₃

Purity: Min. 95%

Molecular weight: 241.24 g/mol

Ref: 3D-RAA77778