79236-82-1

Basic information

• Product Name: 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole
• CAS NO: 79236-82-1
• Molecular Formula: C₁₄H₆N₆O₈S₃
• Molecular Weight: 482.4278
• Mol File: 79236-82-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 714.3°C at 760 mmHg
• Flash Point: 385.8°C
• Density: 1.86g/cm³
• Vapor Pressure: 2.02E-19mmHg at 25°C
• Refractive Index: 1.795
• CAS DataBase Reference: 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole(79236-82-1)
• EPA Substance Registry System: 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole(79236-82-1)

Safety Data

• Hazardous Substances Data: 79236-82-1(Hazardous Substances Data)

Usage

General Description

2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole, also known as Bis(di-2,4-dinitrophenyl)disulfide, is a chemical compound with the molecular formula C14H8N6O8S2. It is a yellow crystalline powder that is insoluble in water but soluble in organic solvents. 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole is often used as a reagent in organic synthesis and as a crosslinking agent for rubber and plastic polymers. It is a versatile compound with diverse applications in the chemical, pharmaceutical, and material science industries. However, it is important to handle this chemical with caution as it is toxic and may cause skin and eye irritation.

Upstream product

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Relevant articles and documents

Synthesis of some novel 1,3,4- and 1,2,4-thiadiazole derivatives

Synthesis and spectral characterization of novel 1,3,4-thiadiazole derivatives including one organo-mercury compound are described. Their structure elucidation was performed by means of spectroscopic and physical methods (IR, 1H NMR, 13/s

Synthesis, 1H NMR Spectral Properties and Conformational Preferences of some Open-chain and Cyclic Aromatic Sulphides Containing Pyridine or 1,3,4-Thiadiazole Units

The conformational preferences in solution of eight new open-chain and cyclic aromatic sulphides containing pyridine or 1,3,4-thiadiazole units have been investigated, parallel to those of some structurally related phenyl sulphides, by means of 1H NMR spectroscopy.The results obtained have shown that replacement of phenyl by the pyridyl or the 1,3,4-thiadiazolyl moieties induces slightly different propeller arrangements, ascribed to the higher conjugative tendency of both electron-deficient heteroaromatic rings, in all open-chain mixed sulphides, in opposition to the skew arrangements observed for phenyl sulphide derivatives.No prominent differences have been found for cyclic sulphides, which preferentially adopt the sterically unhindered saddle shape conformation.