274-30-6

Usage

Uses

Used in Chemical Synthesis:
1,3-Benzodithiol is used as a key intermediate in the synthesis of various organic compounds, including dyes, polymers, and pharmaceuticals. Its reactivity and stability make it a valuable component in the creation of complex molecules and materials.
Used in Dye Production:
1,3-Benzodithiol is used as a precursor in the production of dyes, where its sulfur-containing structure contributes to the color and properties of the final product. This application is crucial in industries such as textiles, where colorfastness and vibrancy are essential.
Used in Polymer Industry:
In the polymer industry, 1,3-benzodithiol is utilized as a monomer or a modifier to enhance the properties of polymers. Its incorporation can improve characteristics such as strength, flexibility, and resistance to environmental factors.
Used in Pharmaceutical Development:
1,3-Benzodithiol is used as a starting material in the development of pharmaceuticals, where its sulfur atoms can form crucial bonds with biological targets. This makes it a promising candidate for the creation of new drugs and therapeutic agents.
Used in Material Science:
1,3-Benzodithiol is employed as a precursor in the manufacturing of various materials, including those with unique electronic, optical, or catalytic properties. Its versatility allows for its use in the development of advanced materials for a range of applications.
Used in Biological and Pharmacological Research:
1,3-Benzodithiol has been studied for its potential biological and pharmacological activities, making it an important subject of research in the scientific community. Its exploration could lead to new discoveries and applications in medicine and healthcare.

Upstream product

• 934-36-1 2-thioxo-1,3-benzodithiole 
• 57842-27-0 1,3-benzodithiol-2-ylium tetrafluoroborate 
• 108-94-1 cyclohexanone 
• 98-86-2 acetophenone 
• 62576-04-9 benzo[d]-1,3-dithiolane-2-one 
• 61666-78-2 2-phenylbenzo--1,3-dithiolane 

Downstream Products

• 112520-09-9 2H-benzo[d][1,3]dithiole 1,1,3,3-tetraoxide 
• 124005-79-4 2--1,3-benzodithiole 
• 68486-94-2 2-methylbenzo[d][1,3]dithiole 
• 670271-13-3 (1R)-[(3S)-methylsulfinyl]methylphenyl sulfoxide 
• 934-36-1 2-thioxo-1,3-benzodithiole 
• 121163-81-3 2-(2-phenethyl)-1,3-benzodithiole-1,1,3,3-tetraoxide 
• 121163-85-7 2-isopropyl-2-(2-phenethyl)-1,3-benzodithiole-1,1,3,3-tetraoxide 
• 121183-90-2 2-cyclohexylmethyl-2-isopropyl-1,3-benzodithiole-1,1,3,3-tetraoxide 
• 121163-86-8 2-(2,2-Dimethyl-propyl)-2-phenethyl-benzo[1,3]dithiole 1,1,3,3-tetraoxide 

Relevant academic research and scientific papers

The facile and direct formylation of organoboron aromatic compounds with benzodithiolylium tetrafluoroborate

Organoboron compounds can be used to effect a direct formylation in the absence of transition metals. We report that the direct reaction between boronic derivatives and benzodithiolylium tetrafluoroborate, a commercially available carbenium ionic compound, is possible and provides access to many interesting compounds without the use of transition metals. The direct reaction of the carbenium ion with boronic derivatives results in the formation of substituted arylcarbenium ions, a number of which can be further utilized in materials chemistry or for the direct transformation into other compounds. In addition to the rich chameleonic chemical nature of the benzodithiol intermediate, such species can also undergo a metallation reaction and subsequent treatment with a wide range of electrophiles to access a variety of functional groups (aldehyde, ketone, acid, and alkyl groups). Copyright

A Convenient Preparation of α-Oxo Ketene Dithioacetals

The reaction of a series of ketones with 2 equiv. of 1,3-benzodithiolylium tetrafluoroborate affords α-(1,3-benzodithiol-2-ylidene)ketones and 1,3-benzodithiole in good yields.

CONVERSION OF CYCLIC TRITHIOCARBONATES TO THIOACETALS, INCLUDING 1,3-DITHIANE, BY REDUCTION WITH DIISOBUTYLALUMINIUM HYDRIDE (DIBAL)

Cyclic trithiocarbonates can be desulfurized with diisobutylaluminium hydride (DIBAL) to form the corresponding thioacetals.This new synthetic pathway was exploited for the preparation of several Umpolung reagents, including 1,3-dithiane.An efficient isolation of sodium trithocarbonate is described.