54815-45-1 Usage
Description
(Ethoxysulfanyl)benzene, also known as ethylthiophenol, is a chemical compound with the formula C8H10OS. It is a colorless to pale yellow liquid characterized by a strong, unpleasant odor. (ethoxysulfanyl)benzene serves as a versatile intermediate in the synthesis of various organic compounds, including pharmaceuticals and fragrances, and plays a significant role in the production of rubber and as a solvent in the manufacture of dyes and chemicals.
Uses
Used in Pharmaceutical Industry:
(Ethoxysulfanyl)benzene is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex organic molecules that possess therapeutic properties.
Used in Fragrance Industry:
In the fragrance industry, (ethoxysulfanyl)benzene is utilized as an intermediate to create various scent compounds, capitalizing on its reactivity to produce a wide array of fragrance notes.
Used in Rubber Production:
(Ethoxysulfanyl)benzene serves as a precursor in the production of rubber, contributing to the development of rubber's chemical structure and properties, which are essential for various applications.
Used as a Solvent in Dye and Chemical Manufacture:
(ethoxysulfanyl)benzene is employed as a solvent in the manufacture of dyes and chemicals, leveraging its solubility properties to facilitate the production process and improve the quality of the final products.
Safety Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 54815-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54815-45:
(7*5)+(6*4)+(5*8)+(4*1)+(3*5)+(2*4)+(1*5)=131
131 % 10 = 1
So 54815-45-1 is a valid CAS Registry Number.
54815-45-1Relevant articles and documents
Synthesis of Sulfinamidines and Sulfinimidate Esters by Transfer of Nitrogen to Sulfenamides
Andresini, Michael,Spennacchio, Mauro,Romanazzi, Giuseppe,Ciriaco, Fulvio,Clarkson, Guy,Degennaro, Leonardo,Luisi, Renzo
, p. 7129 - 7134 (2020/10/02)
In this work we report a new synthetic tactic for the straightforward preparation of hardly accessible sulfinamidines and sulfinamide esters, by using a simple metal-free protocol. The process is robust and uses readily available sulfenamides as the S-don
Experimental Tests of the Stereoelectronic Effect at Phosphorus: Nucleophilic Reactivity of Phosphite Esters
Taira, Kazunari,Mock, William L.,Gorenstein, David G.
, p. 7831 - 7835 (2007/10/02)
Triethyl phosphite rapidly reacts with ethyl benzenesulfenate or diethyl peroxide to yield pentaethoxyphosphorane.In contrast, 1-methyl-4-phospha-3,5,8-trioxabicyclooctane (1) fails to react with either electrophile to yield the expected bicyclic phosphorane 5.The poor reactivity of the bicyclic phosphite 1 is due to a kinetic rather than a thermodynamic barrier because 5 is formed smoothly from an equimolar mixture of P(OEt)5 and the triol 1,1,1-tris(hydroxymethyl)ethane.This result is interpreted in terms of the stereoelectronic effect.The order of nucleophilic reactivity of trialkyl phosphites with 3-benzylidene-2,4-pentanedione is also shown to be consistent with the stereoelectronic effect.The bicyclic phosphite 1 reacted 750 times slower than the pseudoequatorial 2-methoxy ester of hexahydrobenzo-1,3,2-dioxaphosphorinane in a Michael addition reaction with 3-benzylidene-2,4-pentanedione.
