19843-98-2 Usage
Description
[(Cyclohexylsulfanyl)methyl]benzene, also known as cyclohexylmethylbenzenesulfide, is a chemical compound characterized by the molecular formula C13H18S. It presents as a colorless to pale yellow liquid with a distinctive sweet, aromatic scent. [(cyclohexylsulfanyl)methyl]benzene is valued for its versatile applications across different industries due to its unique chemical properties.
Uses
Used in the Chemical Industry:
[(Cyclohexylsulfanyl)methyl]benzene serves as a crucial solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it an indispensable component in the chemical industry. It is used as a solvent for [reason for its use as a solvent, e.g., its ability to dissolve a wide range of substances].
Used in Organic Synthesis:
[(cyclohexylsulfanyl)methyl]benzene also acts as a reagent in organic synthesis, facilitating numerous chemical reactions that lead to the creation of a variety of products. [(Cyclohexylsulfanyl)methyl]benzene is used as a reagent in organic synthesis for [reason for its use as a reagent, e.g., its facilitation of various chemical reactions].
Used in the Perfume Industry:
The sweet, aromatic odor of [(cyclohexylsulfanyl)methyl]benzene makes it a desirable ingredient in the perfume industry. It is used as a base note or modifier in the creation of different fragrances to enhance their complexity and longevity. [(Cyclohexylsulfanyl)methyl]benzene is used as a component in perfumes for [reason for its use, e.g., its sweet, aromatic odor].
Used in the Flavor Industry:
Similarly, its distinctive scent and taste properties position [(cyclohexylsulfanyl)methyl]benzene as a valuable additive in the flavor industry. It can be used to impart specific flavor profiles to various food and beverage products. [(Cyclohexylsulfanyl)methyl]benzene is used as a flavoring agent for [reason for its use, e.g., its distinctive scent and taste properties].
Used in the Pharmaceutical Industry:
[(cyclohexylsulfanyl)methyl]benzene also finds application in the pharmaceutical industry, where it may be used in the development of new drugs or as an intermediate in the synthesis of existing medications. [(Cyclohexylsulfanyl)methyl]benzene is used in the pharmaceutical industry for [reason for its use, e.g., its role in drug development or synthesis].
Used in Polymer Production:
Furthermore, [(cyclohexylsulfanyl)methyl]benzene can be a precursor in the production of polymers, contributing to the development of new materials with specific properties for various applications. It is used as a precursor in polymer production for [reason for its use, e.g., its contribution to the development of new materials].
Safety Precautions:
It is important to handle [(cyclohexylsulfanyl)methyl]benzene with care, as it may pose health risks if ingested, inhaled, or comes into contact with the skin. Appropriate safety measures should be taken during its use to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 19843-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,4 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19843-98:
(7*1)+(6*9)+(5*8)+(4*4)+(3*3)+(2*9)+(1*8)=152
152 % 10 = 2
So 19843-98-2 is a valid CAS Registry Number.
19843-98-2Relevant articles and documents
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Bublitz,D.E.
, p. 1630 - 1631 (1967)
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Transition-Metal-Free and Base-Promoted Carbon-Heteroatom Bond Formation via C-N Cleavage of Benzyl Ammonium Salts
Liu, Long,Tang, Yuanyuan,Wang, Kunyu,Huang, Tianzeng,Chen, Tieqiao
, p. 4159 - 4170 (2021/03/09)
A facile and general method for constructing carbon-heteroatom (C-P, C-O, C-S, and C-N) bonds via C-N cleavage of benzyl ammonium salts under transition-metal-free conditions was reported. The combination of t-BuOK and 18-crown-6 enabled a wide range of substituted benzyl ammonium salts to couple readily with different kinds of heteroatom nucleophiles, i.e. hydrogen phosphoryl compounds, alcohols, thiols, and amines. Good functional group tolerance was demonstrated. The scale-up reaction and one-pot synthesis were also successfully performed.
Efficient visible light initiated hydrothiolations of alkenes/alkynes over Ir2S3/ZnIn2S4: Role of Ir2S3
Li, Yuanyuan,Li, Zhaohui,Wang, Xinglin
, p. 409 - 416 (2020/07/30)
The hydrothiolations of alkynes/alkenes with thiols is an atom-economic and thus attractive method for the constructions of C-S bonds. Here Ir2S3/ZnIn2S4 nanocomposites with varied Ir2S3 loadings were obtained by one-pot solvothermal method from ZnCl2, InCl3 and thioacetamide with IrCl3. The loading of Ir2S3 on the surface of ZnIn2S4 promoted the hydrothiolations of alkenes and alkynes, with an optimum performance observed over 0.5 molpercent Ir2S3/ZnIn2S4 nanocomposite. Based on the studies on the performance of several other cocatalysts (MoS2, NiS and Pd) loaded ZnIn2S4 and the EIS analyses, it was proposed that the superior performance over Ir2S3/ZnIn2S4 nanocomposite can be ascribed to an improved efficiency on the photogeneration of the thiyl radicals by loading Ir2S3 as well as its inactivity for photocatalytic hydrogen evolution, a side reaction in the light initiated hydrothiolation reaction over ZnIn2S4. This study not only demonstrates an efficient and green strategy to synthesize thiolated products under visible light based on semiconductor photocatalysis, but also provides some guidances for the design and development of photocatalytic systems for light induced organic syntheses.
