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Atomfair Benzene, 1-bromo-3-(methylsulfonyl)- m-Bromo(methylsulfonyl)benzene C7H7BrO2S
Description 1-Bromo-3-(methylsulfonyl)benzene (CAS No. 34896-80-5) is a high-purity aromatic sulfone compound with the molecular formula C7H7BrO2S . This white to off-white crystalline solid (MW: 235.10 g/mol) is a versatile building block in organic synthesis, featuring both a reactive bromo substituent and an electron-withdrawing methylsulfonyl group in meta-position. With 98%+ purity by HPLC, it is ideal for nucleophilic substitution reactions, cross-coupling reactions (Suzuki, Stille), and as a precursor for pharmaceuticals and agrochemicals. Packaged under inert gas in amber glass bottles to ensure stability. Technical specifications include: melting point 92-94??C, density 1.55 g/cm3, and storage recommendations at 2-8??C. SDS and Certificate of…
Description
Description
1-Bromo-3-(methylsulfonyl)benzene (CAS No. 34896-80-5) is a high-purity aromatic sulfone compound with the molecular formula C7H7BrO2S. This white to off-white crystalline solid (MW: 235.10 g/mol) is a versatile building block in organic synthesis, featuring both a reactive bromo substituent and an electron-withdrawing methylsulfonyl group in meta-position. With 98%+ purity by HPLC, it is ideal for nucleophilic substitution reactions, cross-coupling reactions (Suzuki, Stille), and as a precursor for pharmaceuticals and agrochemicals. Packaged under inert gas in amber glass bottles to ensure stability. Technical specifications include: melting point 92-94??C, density 1.55 g/cm3, and storage recommendations at 2-8??C. SDS and Certificate of Analysis provided with each order.
- CAS No: 34896-80-5
- Molecular Formula: C7H7BrO2S
- Molecular Weight: 235.10
- Exact Mass: 233.93501
- Monoisotopic Mass: 233.93501
- IUPAC Name: 1-bromo-3-methylsulfonylbenzene
- SMILES: CS(=O)(=O)C1=CC(=CC=C1)Br
- Synonyms: 34896-80-5, Benzene, 1-bromo-3-(methylsulfonyl)-, m-Bromo(methylsulfonyl)benzene, DTXSID50188448, DTXCID80110939
Application
This compound serves as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical research where the methylsulfonyl group enhances metabolic stability. The bromine moiety enables facile functionalization via palladium-catalyzed couplings for drug discovery applications. Researchers also utilize it to create sulfone-containing liquid crystals and advanced materials with tailored electronic properties. Its electron-deficient aromatic ring makes it valuable in designing charge-transfer complexes for optoelectronic applications.
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