Phenyl 4-aminosalicylate, also known as phenyl salicylate or salol, is an organic compound characterized by its ester functional group formed from salicylic acid and phenol. It appears as a white crystalline solid with a slight aromatic odor and is typically insoluble in water but soluble in organic solvents such as ethanol and ether. This compound exhibits properties that make it useful in various applications, including as a UV filter in sunscreens and as a stabilizer in plastics. Additionally, it has been studied for its potential therapeutic effects, particularly in the context of its anti-inflammatory and analgesic properties. The molecular structure features a phenyl group attached to the 4-position of the salicylic acid moiety, which contributes to its chemical reactivity and interactions. Due to its relatively low toxicity, it is often considered safe for use in cosmetic formulations, although care should be taken to avoid excessive exposure. Overall, phenyl 4-aminosalicylate is a versatile compound with significant relevance in both industrial and pharmaceutical contexts.

Phenyl 4-aminosalicylate

133-11-9: 4-Amino-2-hydroxybenzoic acid phenyl ester, 4-Aminosalicylic acid phenyl ester, Benzoic acid, 4-amino-2-hydroxy-, phenyl ester, Fenamisal, NSC 40144, PAS-Tebamin, Pheny-PAS-Tebamin, Phenyl 4-Amino-2-Hydroxybenzoate, Phenyl Aminosalicylate, Phenyl PAS, Phenyl p-aminosalicylate, Phenyl-PAS-Tebamin, Salicylic acid, 4-amino-, phenyl ester, Tebamin, Tebamin-Leo, Tebanyl, p-Aminosalicylic acid phenyl ester, p-Aminosalol,  , 

Phenyl 4-Aminosalicylate

Phenyl4-aminosalicylate is a molecule that has inhibitory properties. It is used in the diagnosis and treatment of various conditions, such as viral infections and cancer. Phenyl4-aminosalicylate binds to the target tissue by means of chemical structures that mimic those found in the cavity. The cavity is an antigen-presenting site on macrophages, which are cells that engulf and digest antigens. Phenyl4-aminosalicylate binds to macrophages via its chemical structure and inhibits the activation of T lymphocytes, thereby preventing activation of immune responses. This drug also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

CAS 133-11-9: Phenyl 4-aminosalicylate

Phenyl 4-Aminosalicylate

Ref: TR-P309020

Phenyl4-aminosalicylate

Ref: 3D-FP151302

Benzoic acid, 4-amino-2-hydroxy-, phenyl ester

Ref: IN-DA0011HH

Phenyl 4-amino-2-hydroxybenzoate

Ref: 10-F435798