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690632-30-5

Benzenesulfonylchloride, 4-(2-methoxyphenoxy)-

Catalog#: AR005MGV  |   CAS#: 690632-30-5  |   MDL#: MFCD01631898  |   MF: C13H11ClO4S  |   MW: 298.7420

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Catalog Number AR005MGV
Chemical Name Benzenesulfonylchloride, 4-(2-methoxyphenoxy)-
CAS Number 690632-30-5
Molecular Formula C13H11ClO4S
Molecular Weight 298.7420
MDL Number MFCD01631898
SMILES COc1ccccc1Oc1ccc(cc1)S(=O)(=O)Cl

4-(2-Methoxyphenoxy)benzene-1-sulfonyl chloride, sometimes referred to as sulfonyl chloride, is a valuable compound commonly used in a variety of chemical synthesis applications. This versatile reagent is renowned for its ability to introduce sulfonyl chloride functional groups into organic molecules, thereby making it an essential tool in building complex molecular structures. One of the primary uses of 4-(2-Methoxyphenoxy)benzene-1-sulfonyl chloride in chemical synthesis is as a sulfonylating agent. By reacting with nucleophiles such as amines, alcohols, or thiols, this compound can facilitate the formation of sulfonamide, sulfonate, or sulfonamide linkages in target molecules. These reactions are crucial in pharmaceutical and agrochemical industries for designing new bioactive compounds and materials with specific properties.Furthermore, sulfonyl chloride derivatives are frequently employed as intermediates in the synthesis of various pharmaceuticals, dyes, and materials. The sulfonyl chloride group's robust nature and reactivity make it a popular choice for modifying organic molecules to enhance their chemical and biological activities. Overall, 4-(2-Methoxyphenoxy)benzene-1-sulfonyl chloride plays a vital role in modern organic synthesis by enabling the construction of diverse chemical structures with tailored properties and functions.
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GHS Pictogram
Signal Word Danger
UN# 3261
Hazard Statements H302-H312-H314-H332
Precautionary Statements P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class 8
Packing Group

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