3-Phenoxybenzoyl chloride, with the CAS number 3586-15-0, is an organic compound characterized by its aromatic structure and the presence of both a phenoxy group and an acyl chloride functional group. It typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. This compound is known for its reactivity, particularly due to the acyl chloride moiety, which can undergo nucleophilic substitution reactions, making it useful in organic synthesis, especially in the preparation of esters and amides. It is also employed in the synthesis of various pharmaceuticals and agrochemicals. The compound is generally handled with care, as it can be corrosive and may cause irritation to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment and working in a well-ventilated area or fume hood, are essential when working with this substance. Its stability is influenced by moisture, as it can hydrolyze to form the corresponding acid.

3-Phenoxybenzoyl chloride

3586-15-0: 3-Phenoxybenzoic acid chloride, Benzoyl chloride, 3-phenoxy-, Benzoyl chloride, m-phenoxy-, m-Phenoxybenzoyl chloride, 3-Phenoxybenzoyl chloride

3-PHENOXYBENZOYL CHLORIDE

3-Phenoxybenzoyl chloride is a type of antiplatelet drug that inhibits the action of platelets. It has been shown to be effective in inhibiting the production of thromboxane A2, which is an important mediator in the formation of blood clots. 3-Phenoxybenzoyl chloride blocks the receptor for angiotensin, thereby reducing its ability to cause vasoconstriction and increasing blood flow. This drug also has a number of other activities including inhibition of prostaglandin synthesis, antagonistic effects at GABA receptors, and interference with the function of ion channels.

CAS 3586-15-0: 3-Phenoxybenzoyl chloride

3-Phenoxybenzoyl chloride

Ref: 10-F014703

3-PHENOXYBENZOYL CHLORIDE

Ref: IN-DA00C8FA

3-Phenoxybenzoyl chloride

Ref: 54-OR9642

3-Phenoxybenzoyl chloride

Ref: 3D-DAA58615