4132-56-3

Basic information

• Product Name: 1,3-Dithiolane-4,5-dione, 2-thioxo-
• CAS NO: 4132-56-3
• Molecular Formula: C3O2S3
• Molecular Weight: 0.00000
• Mol File: 4132-56-3.mol
• Article Data: 0

Chemical Properties

• Melting Point: 66 °C(Solv: hexane (110-54-3))
• Boiling Point: 90 °C(Press: 2 Torr)
• Density: 1 g/cm3(Temp: 25 °C)
• CAS DataBase Reference: 1,3-Dithiolane-4,5-dione, 2-thioxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiolane-4,5-dione, 2-thioxo-(4132-56-3)
• EPA Substance Registry System: 1,3-Dithiolane-4,5-dione, 2-thioxo-(4132-56-3)

Safety Data

• Hazardous Substances Data: 4132-56-3(Hazardous Substances Data)

Usage

Explanation

A heterocyclic compound is a ring-shaped molecule containing atoms of different elements. In this case, the ring has four members (atoms) and includes carbon, sulfur, and oxygen atoms.
3. Contains two sulfur atoms and two oxygen atoms

Explanation

The compound's structure includes two sulfur (S) atoms and two oxygen (O) atoms, which contribute to its unique properties and reactivity.
4. Potent biological properties

Explanation

1,3-Dithiolane-4,5-dione, 2-thioxohas been found to possess significant biological activities, such as antioxidant and antifungal properties.
5. Antioxidant activity

Explanation

The compound has the ability to neutralize harmful free radicals, protecting cells from oxidative damage and potentially reducing the risk of various diseases.
6. Antifungal activity

Explanation

It has been shown to inhibit the growth of certain fungi, making it a potential candidate for use in antifungal treatments.
7. Potential use in pharmaceuticals

Explanation

Due to its biological properties, 1,3-Dithiolane-4,5-dione, 2-thioxomay be developed into a pharmaceutical compound for treating various conditions.
8. Building block in organic synthesis

Explanation

The compound can be used as a starting material or intermediate in the synthesis of more complex organic molecules.
9. Role in chemical reactions

Explanation

1,3-Dithiolane-4,5-dione, 2-thioxohas been investigated for its participation in various chemical reactions, contributing to the understanding of its reactivity and potential applications.
10. Potent reagent in organic chemistry

Explanation

The compound's unique structure and reactivity make it a valuable reagent in organic chemistry, potentially leading to the development of new synthetic methods and compounds.

Downstream Products

• 4216-77-7 2.2-Diphenyl.1.4.7-trithia-spiro<2.4>heptandion-(5.6) 
• 88691-98-9 5,5-diphenyl-4,2'-spirobis[1,3-dithiolane]-4',5'-dione