Benzoyl chloride, 2-mercapto- is an organic compound characterized by the presence of both a benzoyl chloride functional group and a thiol (-SH) group. It typically appears as a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity. The compound is known for its ability to participate in nucleophilic substitution reactions, where the thiol group can act as a nucleophile, making it useful in various synthetic applications, particularly in the preparation of thioesters and other sulfur-containing compounds. It is also sensitive to moisture and can hydrolyze in the presence of water, releasing hydrochloric acid. Due to its reactivity, proper handling and storage in a controlled environment are essential to prevent unwanted reactions. Safety precautions are necessary, as it can be corrosive and irritating to the skin, eyes, and respiratory system. Overall, benzoyl chloride, 2-mercapto- is a valuable intermediate in organic synthesis, particularly in the field of medicinal chemistry and materials science.

Benzoyl chloride, 2-mercapto-

1677-25-4: Benzoyl chloride, 2-mercapto- is an organic compound characterized by the presence of both a benzoyl chloride functional group and a thiol (-SH) group. It typically appears as a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity. The compound is known for its ability to participate in nucleophilic substitution reactions, where the thiol group can act as a nucleophile, making it useful in various synthetic applications, particularly in the preparation of thioesters and other sulfur-containing compounds. It is also sensitive to moisture and can hydrolyze in the presence of water, releasing hydrochloric acid. Due to its reactivity, proper handling and storage in a controlled environment are essential to prevent unwanted reactions. Safety precautions are necessary, as it can be corrosive and irritating to the skin, eyes, and respiratory system. Overall, benzoyl chloride, 2-mercapto- is a valuable intermediate in organic synthesis, particularly in the field of medicinal chemistry and materials science.

CAS 1677-25-4

Benzoyl chloride, 2-mercapto-

2-Mercaptobenzoyl chloride

Ref: 54-OR46677