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Merck
CN

392391

二对甲苯酰硫

99%

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关于此项目

线性分子式:
(CH3C6H4)2SO2
化学文摘社编号:
分子量:
246.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-969-6
MDL number:
Assay:
99%
Form:
solid
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Quality Level

assay

99%

form

solid

mp

158-160 °C (lit.)

solubility

chloroform: soluble 25 mg/mL, clear, colorless to yellow

functional group

sulfone

SMILES string

Cc1ccc(cc1)S(=O)(=O)c2ccc(C)cc2

InChI

1S/C14H14O2S/c1-11-3-7-13(8-4-11)17(15,16)14-9-5-12(2)6-10-14/h3-10H,1-2H3

InChI key

WEAYCYAIVOIUMG-UHFFFAOYSA-N

General description

Di-p-tolyl sulfone is a di-p-substituted diaryl sulfone. Its synthesis by the sulfonylation of toluene with p-toluenesulfonic acid (TsOH) in the presence of polystyrene supported aluminium triflate (Ps-Al(OTf)3) catalyst has been reported along with its NMR and IR spectra. The gas-phase heats of formation of di-p-tolyl sulfone has been studied. The kinetics and thermodynamics of sulphuric acid assisted cleavage of di-p-tolyl sulfone has been invesitigated.

Application

Di-p-tolyl sulfone may be used in the synthesis of isomeric p-tolylpyridines (α , β and γ ) by photochemical decomposition.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Studies in the thermochemistry of sulphones. Part 6.-Heats of combustion, fusion, vaporization and atomization of six aromatic and two allylic sulphones.
Mackle H and O'Hare PAG.
Transactions of the Faraday Society, 57, 1521-1526 (1961)
Kinetics and thermodynamics of sulfuric acid-mediated cleavage of substituted diaryl sulfones.
Ward RS, et al.
Journal of Surfactants and Detergents, 4(2), 185-190 (2001)
Polystyrene Supported Al (OTf)3: a Stable, Efficient, Selective, and Reusable Catalyst for Sulfonylation of Arenes with Sulfonic Acids.
Boroujeni, KP.
Bull. Korean Chem. Soc., 31(7), 1887-1890 (2010)



全球贸易项目编号

货号GTIN
392391-100G04061832425214