3'-(Trifluoromethyl)biphenyl-4-sulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. This compound typically appears as a solid or liquid, depending on the specific conditions, and is often handled with care due to its potential reactivity, particularly with nucleophiles, which can lead to the formation of sulfonamides or other derivatives. Its sulfonyl chloride moiety is particularly useful in acylation reactions, allowing for the introduction of sulfonyl groups into various substrates. Additionally, the biphenyl structure contributes to the compound's stability and can affect its solubility in organic solvents. As with many sulfonyl chlorides, it is important to consider safety precautions when handling this compound, as it can be corrosive and may release toxic gases upon reaction with water or moisture.

3'-(trifluoromethyl)biphenyl-4-sulfonyl chloride

885267-96-9: 3'-(Trifluoromethyl)biphenyl-4-sulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. This compound typically appears as a solid or liquid, depending on the specific conditions, and is often handled with care due to its potential reactivity, particularly with nucleophiles, which can lead to the formation of sulfonamides or other derivatives. Its sulfonyl chloride moiety is particularly useful in acylation reactions, allowing for the introduction of sulfonyl groups into various substrates. Additionally, the biphenyl structure contributes to the compound's stability and can affect its solubility in organic solvents. As with many sulfonyl chlorides, it is important to consider safety precautions when handling this compound, as it can be corrosive and may release toxic gases upon reaction with water or moisture.

CAS 885267-96-9

3'-(trifluoromethyl)biphenyl-4-sulfonyl chloride

3′-(trifluoromethyl)biphenyl-4-sulfonyl chloride

Ref: 10-F496469