5432-98-4 Usage
Description
[2-(dodecylsulfanyl)ethyl]benzene, also known as bis(2-dodecylthioethyl)benzene, is a chemical compound belonging to the aromatic compounds family. It is derived from benzene and features a benzene ring with a 2-(dodecylsulfanyl)ethyl group attached, which contributes to its various applications in industrial and consumer products.
Uses
Used in Lubricants:
[2-(dodecylsulfanyl)ethyl]benzene is used as an additive in the lubricant industry to enhance the performance and efficiency of lubricants. Its chemical structure allows it to improve the lubricating properties and reduce friction between moving parts, leading to better machinery operation and reduced wear.
Used in Solvents:
In the solvent industry, [2-(dodecylsulfanyl)ethyl]benzene is utilized as a component in the formulation of various solvents. Its aromatic nature and the presence of the 2-(dodecylsulfanyl)ethyl group make it suitable for dissolving a wide range of substances, making it a valuable addition to the solvent formulations.
Used in Plasticizers:
[2-(dodecylsulfanyl)ethyl]benzene is also employed in the production of plasticizers, which are additives used to increase the flexibility and workability of plastics. Its chemical properties enable it to improve the plasticity and processability of various polymers, resulting in better end products with enhanced properties.
Used in Specialty Chemicals:
[2-(dodecylsulfanyl)ethyl]benzene serves as a component in the synthesis of specialty chemicals, which are high-value chemicals used in various applications, including pharmaceuticals, agrochemicals, and materials science. Its unique structure and properties make it a valuable building block for the development of novel specialty chemicals.
Used in Pharmaceutical Drug Synthesis:
In the pharmaceutical industry, [2-(dodecylsulfanyl)ethyl]benzene is used as an intermediate in the synthesis of various drugs. Its aromatic and sulfur-containing structure can be further modified and functionalized to create active pharmaceutical ingredients with specific therapeutic properties.
Used in Environmental and Biological Impact Studies:
[2-(dodecylsulfanyl)ethyl]benzene has been studied for its potential as an endocrine disruptor, which can have significant biological and environmental impacts. Understanding its effects on ecosystems and human health is crucial for developing appropriate handling, use, and disposal protocols to minimize its potential negative impact.
Check Digit Verification of cas no
The CAS Registry Mumber 5432-98-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5432-98:
(6*5)+(5*4)+(4*3)+(3*2)+(2*9)+(1*8)=94
94 % 10 = 4
So 5432-98-4 is a valid CAS Registry Number.
5432-98-4Relevant articles and documents
Regioselectivity of Radical Addition of Thiols to 1-Alkenes
Biermann, Ursula,Metzger, Jürgen O.
, p. 730 - 734 (2018)
The addition of dodecanethiol (1) to 1-alkenes H2C=CHR that have substituents R = Hex, (CH2)8COOMe, Ph, Bn, cHex, CH2cHex, tBu (2a–2g) with different steric effects was studied. Some few percent of branched Mark
Visible light initiated hydrothiolation of alkenes and alkynes over ZnIn2S4
Li, Yuanyuan,Cai, Jingyu,Hao, Mingming,Li, Zhaohui
, p. 2345 - 2351 (2019/05/21)
The construction of C-S bonds is very important. The hydrothiolation of alkenes or alkynes with thiols represents an attractive and atom economical approach for the formation of C-S bonds. In this manuscript, flowerlike microspheres of ZnIn2S4 consisting of interweaving nanoflakes were prepared by a solvothermal method and were applied for the first time in the visible light initiated hydrothiolation of alkenes and alkynes. The reactions between a broad range of thiols and alkynes or alkenes over irradiated ZnIn2S4 afford the corresponding hydrothiolated products in moderate to excellent yields. The mechanism proposed based on the ESR results suggests that the holes generated over irradiated ZnIn2S4 are reductively quenched by the thiols to generate thiyl radicals, which are added to the alkynes/alkenes to generate alkene/alkyl radicals for the propagation of thiol-ene/thiol-yne coupling reactions. The use of solar light and a semiconductor-based photocatalyst to realize the thiol-ene and thiol-yne coupling reactions in a green solvent (methanol), with only stoichiometric thiols required and applicable to a broad substrate scope, makes this reaction protocol a green, sustainable and cost-effective strategy for the synthesis of thiolated products. This study also highlights the great potential of semiconductor-based photocatalysis for advanced organic syntheses.
