Description

Methylene bis(4-methylbenzenesulfonate) (CAS No. 24124-59-2) is a high-purity organic compound with the molecular formula C₁₅H₁₆O₆S₂. This specialized chemical, also known by its IUPAC name (4-methylphenyl)sulfonyloxymethyl 4-methylbenzenesulfonate, is a bis-sulfonate ester derivative widely utilized in organic synthesis and material science applications. The compound features two toluene sulfonate groups linked by a methylene bridge, offering unique reactivity as a crosslinking agent or electrophile. Our product is rigorously tested to ensure exceptional purity and consistency, making it ideal for demanding research applications. Supplied as a crystalline solid with detailed technical specifications, this reagent is suitable for use in pharmaceutical intermediates, polymer chemistry, and advanced material development. Each batch is accompanied by comprehensive analytical data including HPLC, NMR, and mass spectrometry results to guarantee quality and reproducibility for your scientific work.

Properties

• CAS Number: 24124-59-2
• Complexity: 504
• IUPAC Name: p-tolylsulfonyloxymethyl 4-methylbenzenesulfonate
• InChI: InChI=1S/C15H16O6S2/c1-12-3-7-14(8-4-12)22(16,17)20-11-21-23(18,19)15-9-5-13(2)6-10-15/h3-10H,11H2,1-2H3
• InChI Key: LEXULLPDKRNGQG-UHFFFAOYSA-N
• Exact Mass: 356.03883057
• Molecular Formula: C15H16O6S2
• Molecular Weight: 356.4
• SMILES: CC1=CC=C(C=C1)S(=O)(=O)OCOS(=O)(=O)C2=CC=C(C=C2)C
• Topological: 104
• Monoisotopic Mass: 356.03883057
• Synonyms: 24124-59-2, Methylene bis(4-methylbenzenesulfonate), METHYLENE BIS(TOLUENE-4-SULFONATE), 1-methyl-4-[(4-methylphenyl)sulfonyloxymethoxysulfonyl]benzene, (4-methylphenyl)sulfonyloxymethyl 4-methylbenzenesulfonate, MFCD10568564, Bis(tosyloxy)methane, Methanediol, di-p-toluenesulfonate, C15H16O6S2, Methanediol, bis(4-methylbenzenesulfonate), SCHEMBL3315459, CHEMBL1983147, DTXSID30317572, LEXULLPDKRNGQG-UHFFFAOYSA-N, BBL100521, NSC318486, STL554315, Methylenebis(4-methylbenzenesulfonate), AKOS005167037, NSC-318486, methanediyl bis(4-methylbenzenesulfonate), MS-20031, NCI60_002733, DB-430523, Methylene bis(4-methylbenzene-1-sulfonate), CS-0153013, D83549, Methanediol, 1,1-bis(4-methylbenzenesulfonate), {[(4-METHYLPHENYL)SULFONYL]OXY}METHYL 4-METHYLBENZENESULFONATE

Application

Methylene bis(4-methylbenzenesulfonate) serves as a versatile reagent in organic synthesis, particularly useful as a bifunctional alkylating agent for creating molecular bridges in complex architectures. In polymer chemistry, it acts as an effective crosslinker for modifying material properties through sulfonate ester linkages. Researchers employ this compound in pharmaceutical intermediate synthesis where its dual reactive sites enable controlled molecular scaffolding. The reagent also finds application in the development of specialty chemicals requiring precise sulfonate functionalization.

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