31350-39-7

Basic information

• Product Name: Benzene, 1-[(dibromomethyl)sulfonyl]-4-methyl-
• CAS NO: 31350-39-7
• Molecular Formula: C8H8Br2O2S
• Molecular Weight: 328.024
• Mol File: 31350-39-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(dibromomethyl)sulfonyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(dibromomethyl)sulfonyl]-4-methyl-(31350-39-7)
• EPA Substance Registry System: Benzene, 1-[(dibromomethyl)sulfonyl]-4-methyl-(31350-39-7)

Safety Data

• Hazardous Substances Data: 31350-39-7(Hazardous Substances Data)

Upstream product

• 3937-96-0 tosylacetic acid 
• 7732-18-5 water 
• 7726-95-6 bromine 
• 766-40-5 Mucochloric acid 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 766-38-1 mucobromic acid 
• 767-97-5 3,4-dibromo-5-methoxy-2,5-dihydrofuran-2-one 
• 67-68-5 dimethyl sulfoxide 
• 1193-82-4 racemic methyl phenyl sulfoxide 
• 52345-47-8 p-tolylsulphonylacetamide 
• 56-23-5 tetrachloromethane 
• 75-25-2 Bromoform 

Downstream Products

• 139950-96-2 (Z)-2-methyl-1-p-tolylsulfonyl-1-butene 
• 139950-95-1 (E)-2-methyl-1-p-tolylsulfonyl-1-butene 
• 136828-02-9 <(p-Tolylsulfonyl)methylene>cyclohexane 
• 58202-58-7 (Z)-2-methyl-1-p-tolylsulfonyl-1-hexene 

Relevant articles and documents

Based on 3, 4 - dihalo -2 (5H) - furanone preparation two effluent-based aryl or hetero-aromatic sulfone method

The invention relates to a method for preparing dihalogen methyl aryl sulfone based on 3,4-dihalogen-2(5H)-furanone. The preparation method comprises the following step: by taking 3,4-dihalogen-2(5H)-furanone compounds, sodium arylsulfinate and dimethyl s

Chemoselective mono halogenation of β-keto-sulfones using potassium halide and hydrogen peroxide; synthesis of halomethyl sulfones and dihalomethyl sulfones

The synthesis of α-halo β-keto-sulfones using potassium halide and hydrogen peroxide as a chemoselective mono halogenation reagent and the synthesis of α,α-symmetrical and asymmetrical dihalo β-keto-sulfones and α-halo, α-alkyl and β-keto-sulfones is described. Base induced cleavage of α-halo β-keto-sulfones, α,α-dihalo β-keto-sulfones, and α-halo, α-alkyl β-keto-sulfones afforded the corresponding halomethyl sulfones, dihalomethyl sulfones and haloalkyl sulfones.