274-30-6

Basic information

• Product Name: 1,3-BENZODITHIOL
• Synonyms: 1,3-BENZODITHIOL;1,3-Benzodithiole
• CAS NO: 274-30-6
• Molecular Formula: C₇H₆S₂
• Molecular Weight: 154.25
• Mol File: 274-30-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 104-106 °C(Press: 2 Torr)
• Appearance: /
• Density: 1.312±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-BENZODITHIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-BENZODITHIOL(274-30-6)
• EPA Substance Registry System: 1,3-BENZODITHIOL(274-30-6)

Safety Data

• Hazardous Substances Data: 274-30-6(Hazardous Substances Data)

Usage

General Description

1,3-Benzodithiol is a chemical compound with the molecular formula C4H4S2. It is a sulfur-containing aromatic compound that is commonly used as a building block in organic synthesis. 1,3-Benzodithiol has a wide range of applications in the preparation of dyes, polymers, and pharmaceuticals. It is also used as a precursor in the manufacturing of various chemicals and materials. Additionally, 1,3-benzodithiol has been studied for its potential biological and pharmacological activities, making it a versatile and important chemical in various industries.

Upstream product

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

Downstream Products

• 124005-79-4 2--1,3-benzodithiole 
• 68486-94-2 2-methylbenzo[d][1,3]dithiole 
• 112520-09-9 2H-benzo[d][1,3]dithiole 1,1,3,3-tetraoxide 
• 934-36-1 2-thioxo-1,3-benzodithiole 

Relevant articles and documents

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

REDUKTION VON 1,3-BENZODITHIOL-2-THIONEN BZW. SELONEN MIT HYDRIDEN

-