112520-09-9

Basic information

• Product Name: Benzo[1,3]dithiole 1,1,3,3-tetraoxide
• Synonyms: Benzo[1,3]dithiole 1,1,3,3-tetraoxide;1,3-Benzodithiole, 1,1,3,3-tetraoxide
• CAS NO: 112520-09-9
• Molecular Formula: C₇H₆O₄S₂
• Molecular Weight: 218.25014
• Mol File: 112520-09-9.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzo[1,3]dithiole 1,1,3,3-tetraoxide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo[1,3]dithiole 1,1,3,3-tetraoxide(112520-09-9)
• EPA Substance Registry System: Benzo[1,3]dithiole 1,1,3,3-tetraoxide(112520-09-9)

Safety Data

• Hazardous Substances Data: 112520-09-9(Hazardous Substances Data)

Usage

General Description

Benzo[1,3]dithiole 1,1,3,3-tetraoxide, also known as BEDT, is a chemical compound with a unique structure containing four sulfur atoms and a benzene ring. It is a redox-active molecule that has attracted attention in the field of materials science and organic electronics due to its potential for use in conducting polymers and organic semiconductors. BEDT exhibits interesting properties such as high conductivity, stability, and the ability to undergo reversible redox reactions, making it a promising candidate for applications in electronic devices and energy storage. Additionally, it has shown potential for use in drug development due to its antioxidant and anti-inflammatory properties. However, the chemical's low solubility and limited synthetic methods present challenges to its widespread use, and further research is needed to fully understand and harness its potential.

Upstream product

• 108-98-5 thiophenol 
• 62217-32-7 2-diphenylmethylene-1,3-benzodithiole 
• 17534-15-5 Benzene-1,2-dithiol 
• 274-30-6 1,3-benzodithiol 
• 112520-04-4 2-diphenylmethylene-1,3-benzodithiole 1,1,3,3-tetraoxide 

Downstream Products

• 1221907-18-1 2-fluoro-2-(hydroxyphenylmethyl)-1,3-benzodithiole-1,1,3,3-tetraoxide 
• 1380569-71-0 2-(4-methoxyphenyl)methylene-1,3-benzodithiole 1,1,3,3-tetroxide 
• 1381793-43-6 2-benzylidene-1,3-benzodithiole 1,1,3,3-tetroxide 
• 1381793-57-2 3-((4-methoxyphenyl)(1,1,3,3-tetraoxidobenzo[d][1,3]dithiol-2-yl)methyl)pentane-2,4-dione 
• 1381793-56-1 diethyl 2-((4-methoxyphenyl)(1,1,3,3-tetraoxidobenzo[d][1,3]dithiol-2-yl)methyl)malonate 
• 1381793-55-0 3-(phenyl(1,1,3,3-tetraoxidobenzo[d][1,3]dithiol-2-yl)methyl)pentane-2,4-dione 

Relevant articles and documents

Cross-Dehydrogenative Coupling of Tetrahydroisoquinolines and 2-Fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide: A New Synthetic Approach to α-Monofluoromethyl Tertiary Amines

A cross dehydrogenative coupling reaction of tetrahydroisoquinolines with 2-fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide had been developed. CuBr/TBHP was identified as the best catalyst and oxidant. A variety of coupling products were obtained with good t

2-FLUORO-1,3-BENZODITHIOL 1,1,3,3-TETRAOXIDE DERIVATIVE, PRODUCTION METHOD THEREOF, AND PRODUCTION METHOD OF MONOFLUOROMETHYL GROUP-CONTAINING COMPOUND USING THE SAME

A 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative as a monofluoromethyl group introduction agent that is effective as an intermediate in pharmaceutical and agrochemical synthesis, a production method thereof, and a production method of a monofluoromethyl group-containing compound using this 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative are provided. The 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative represented by the following general formula (1) (wherein R1, R2, R3, and R4 each independently represent a hydrogen atom, a straight-chain or branched alkyl group having 1 to 4 carbon atoms, a straight-chain or branched alkyloxy group having 1 to 4 carbon atoms, a halogen atom, a nitro group, or a cyano group), the production method thereof, and various monofluoromethyl group-containing compounds are manufactured using this 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative as a monofluoromethylating agent.

1,3-BENZODITHIOLE TETRAOXIDE AS A CH2(2-) SYNTHON

1,3-Benzodithiole tetraoxide (BDT) 4 is more reactive in alkylation reactions than the commonly used bis(benzenesulfonyl)methane (1).This is demonstrated notably in dialkylations with sterically demanding alkyl halides.Besides its ready access and larger