4'-Methoxybiphenyl-4-sulfonyl chloride, with the CAS number 202752-04-3, is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a biphenyl structure that has a methoxy substituent. This compound typically appears as a solid at room temperature and is known for its reactivity due to the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. The methoxy group enhances the compound's solubility in organic solvents and can influence its electronic properties, making it useful in various synthetic applications, particularly in the preparation of sulfonamide derivatives. Additionally, the compound may exhibit moderate to high stability under standard conditions but should be handled with care due to the potential release of hydrochloric acid upon hydrolysis. Its applications are often found in pharmaceuticals and agrochemicals, where it serves as an important intermediate in the synthesis of more complex molecules. Proper safety measures should be observed when working with this compound due to its reactive nature.

4'-methoxybiphenyl-4-sulfonyl chloride

202752-04-3: [1,1'-Biphenyl]-4-sulfonyl chloride, 4'-methoxy-, 4'-Methoxy-1,1'-Biphenyl-4-Sulfonyl Chloride,  4'-Methoxybiphenyl-4-sulfonyl chloride

[1,1'-Biphenyl]-4-sulfonyl chloride, 4'-methoxy-

4'-Methoxy-biphenyl-4-sulfonyl chloride

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[4-(4-Methoxyphenyl)phenyl]sulphonyl chloride

CAS 202752-04-3: 4'-methoxybiphenyl-4-sulfonyl chloride

[1,1'-Biphenyl]-4-sulfonyl chloride, 4'-methoxy-

Ref: IN-DA0028E1

4'-Methoxy-biphenyl-4-sulfonyl chloride

Ref: 10-F034250

4'-Methoxy-biphenyl-4-sulfonyl chloride

Ref: 3D-FM52974

[4-(4-Methoxyphenyl)phenyl]sulphonyl chloride

Ref: 54-OR12664