5409-96-1

Usage

Explanation

The compound is composed of 16 carbon atoms, 16 hydrogen atoms, 2 chlorine atoms, and 2 sulfur atoms.

Explanation

The core structure of the compound is a benzene ring, which is a six-carbon ring with alternating single and double bonds. A chlorine atom is attached at the first position (1-chloro), and two sulfur-containing groups are connected to the benzene ring.

Explanation

The compound is classified as a chlorinated aromatic compound because it has a chlorine atom (Cl) attached to the benzene ring.

Explanation

The compound has two sulfur atoms (S) as part of its functional groups, which are connected to the benzene ring through carbon chains.

Explanation

Due to its unique structure and properties, the compound can be used as a building block or intermediate in the synthesis of a wide range of organic compounds and materials. It may also have potential applications in the development of new drugs, agrochemicals, and other products in various industries.

Explanation

The compound's structure is unique due to the presence of both chlorine and sulfur atoms, which can influence its reactivity, stability, and potential applications in different fields.

Explanation

The material does not provide information about the compound's physical properties, such as melting point, boiling point, density, or solubility.

Explanation

The material does not provide information about the compound's chemical properties, such as reactivity, stability, or potential reactions with other compounds.

Explanation

The material does not provide information about the safety precautions or handling procedures for 1-CHLORO-4-((4-[(4-CHLOROPHENYL)SULFANYL]BUTYL)SULFANYL)BENZENE. It is essential to follow proper safety protocols when working with chemicals, especially if they are toxic, corrosive, or reactive.

Molecular Structure

Benzene ring with a chlorine atom at position 1 and two sulfur-containing groups attached

Chlorinated Aromatic Compound

Contains a chlorine atom

Sulfur-Containing Functional Groups

Two sulfur atoms in the molecule

Potential Applications

Synthesis of various organic compounds and materials, pharmaceuticals, agrochemicals, and other industries

Unique Structure

Presence of chlorine and sulfur atoms in the molecule

Physical Properties

Not provided in the material

Chemical Properties

Not provided in the material

Safety and Handling

Not provided in the material

Upstream product

• 106-54-7 p-Chlorothiophenol 
• 110-56-5 1,4-dichlorobutane 
• 109-99-9 tetrahydrofuran 
• 110-52-1 1,4-dibromo-butane 

Downstream Products

• 145917-53-9 C₁₆H₁₆Cl₂O₄S₂ 

Relevant academic research and scientific papers

Ionic liquid as catalyst and reaction medium: A simple, convenient and green procedure for the synthesis of thioethers, thioesters and dithianes using an inexpensive ionic liquid, [pmIm]Br

An easily accessible and inexpensive room temperature ionic liquid, 1-pentyl-3-methylimidazolium bromide, [pmIm]Br efficiently catalyzes the reaction of alkyl halides or acyl halides with thiols without any solvent at room temperature leading to the synthesis of thioethers and thioesters in high yields. This reaction has also been extended for the preparation of dithianes and transthioetherification. The ionic liquid is recovered and recycled for subsequent runs.

Unusual cleavage of ethers by thiophenol on the surface of silica gel impregnated with indium(III) chloride under microwave irradiation: Efficient procedure for the synthesis of thioethers through transthioetherification

Cyclic and open-chain benzylic ethers undergo cleavage by thiophenol on the surface of silica gel impregnated with indium(III) chloride under microwave irradiation to produce the corresponding di- and monothioethers.

1H- And13C-NMR and electron ionization (EI) mass spectrometric study of o- And p-substituted 1,n-diarylsulfonylalkanes, XC6H4so2(CH2)nso 2C6H4X (n = 2-5, 8, 10)+

1,n-Diphenylsulfonylalkanes, PhSO2(CH2)nSO2Ph (n =2-5, 8, 10) and their o- or p-Cl or -OMe derivatives were prepared and their 1H- and 13C-NMR and EI mass spectra recorded and analyzed. The chemical shifts of the aliphatic α- and β-carbons showed a clear dependence on the o-aryl substitution, the o-Cl being the most shielding for both. Clear low-field effects were found also for the aliphatic α-protons in o-Cl and o-OMe derivatives. In case of p-OMe derivatives a palpable shielding of the aliphatic α-protons was also found similarly to the β-protons of the o-OMe derivatives. Characteristic mass spectrometric fragmentations which reflected both the influence of the aryl substitution and the length of the alkyl chain were observed and sometimes also exhibited the sulphinic acid rearrangement.

INNOVATIVE APPROACH TO THE SYNTHESIS OF SULPHIDES AND THEIR CORRESPONDING SULPHONES

A general and efficient synthetic approach to aryl-aryl bis-sulphides with aliphatic or aromatic bridges via the nucleophilic aromatic substitution (SNAr) of cyclopentadienyliron arene complexes with a number of dithiols followed by photolytic demetallation is presented in this work.The oxidation of the bis(cyclopentadienyliron) arene complexes containing bis-sulphide linkages with 3-chlorobenzoic acid gave their corresponding sulphones in very good yield (70-95percent).Mixed ether/sulphide and ether/sulphone complexes were also prepared following the same synthetic strategy.Reactions of sulphide and sulphone diiron complexes with terminal chloro groups with a number of oxygen, sulphur and carbon nucleophiles allowed for the functionalization of these complexes.The use of photolytic demetallation as a means of liberating the modified arene ligands proved to be very successful.The mild conditions, high yields and low cost of the starting iron complexes make this method one of the most general and practical routes to sulphide and sulphone compounds.

Dipole Moments and UV Spectra of some Long-chain Molecules

About one hundred compounds with long-chain molecular structure have been prepared (most of them are new).The dipole moments of four α,ω-bis(p-methoxyphenylthio)alkanes and five α,ω-bis(p-methoxyphenylsulphonyl)alkanes have been determined to find the effect of chain-length.In the case of sulphones, the observed values are compared with the values calculated for free rotation around all bonds intervening the end dipoles.The uv spectra of some 1,2-(distyrylsulphonyl)ethanes, and a number of α,ω-bis(arylsulphonyl)- and α,ω-bis(aryloxy)alkanes have been recorded to examine the applicability of the principle of chromophore additivity.