4946-13-8 Usage
Description
4-Ethylthiophenol, also known as 4-(ethylthio)phenol, is an organic compound with the chemical formula C6H4SH(CH2CH3). It is a colorless to pale yellow liquid and is a useful research chemical due to its unique chemical properties.
Uses
Used in Research and Development:
4-Ethylthiophenol is used as a research chemical for various applications in the field of chemistry and material science. Its unique properties make it a valuable compound for studying and developing new materials, pharmaceuticals, and other chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Ethylthiophenol is used as an intermediate in the synthesis of various drugs and drug candidates. Its chemical structure allows for further modification and functionalization, making it a versatile building block in the development of new medications.
Used in Chemical Synthesis:
4-Ethylthiophenol is also used as a starting material or intermediate in the synthesis of various organic compounds, including specialty chemicals, dyes, and additives. Its reactivity and functional groups make it a useful component in the creation of complex molecules and materials.
Used in Material Science:
In the field of material science, 4-Ethylthiophenol can be used to develop new materials with specific properties, such as improved conductivity, enhanced stability, or unique optical characteristics. Its incorporation into polymers, composites, or other materials can lead to the creation of novel products with a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4946-13-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4946-13:
(6*4)+(5*9)+(4*4)+(3*6)+(2*1)+(1*3)=108
108 % 10 = 8
So 4946-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10S/c1-2-7-3-5-8(9)6-4-7/h3-6,9H,2H2,1H3/p-1
4946-13-8Relevant articles and documents
The Reaction of Alkyl-substituted Thioanisoles with PCl3 and AlCl3: a Route to Benzothiadiphospholobenzothiadiphosphole Derivatives
Baccolini, Graziano,Mezzina, Elisabetta,Todesko, Paolo Edgardo
, p. 3281 - 3284 (2007/10/02)
The synthesis of benzothiadiphospholobenzothiadiphosphole derivatives starting from alkyl-substituted thioanisoles and PCl3-AlCl3 is reported.The reaction is carried out at reflux in the absence of solvent and the yields are dependent on the starting sulphide.These new heterocycles can be purified by simple filtration on a Florisil column and have been characterized by 1H-, 13C-, (1H)31P-n.m.r. and mass spectroscopy analyses.New unexpected findings are also described.
MOESSBAUER AND NUCLEAR MAGNETIC RESONANCE SPECTROSCOPIC STUDIES ON 'MYOCRISIN', 'SOLGANOL', 'AURANOFIN', AND RELATED GOLD(I) THIOLATES
Al-Sa'ady, Ali K. H.,Moss, Karen,McAuliffe, Charles A.,Parish, R. V. ("Dick")
, p. 1609 - 1616 (2007/10/02)
A large number of gold(I) thiolates, , have been prepared in which the R group is an alkyl, aryl, carboxylic acid, amino acid, or heterocycle.Most are highly insoluble in all common solvents, but (R' = Et, iPr, sBu, or tBu) dissolv
Antiallergic cyclic sulphur compounds
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, (2008/06/13)
Certain tricyclic thioxanthone-10,10-dioxide compounds each of which is substituted in the 1-,2-,3- or 4-position by a carboxyl or (5-tetrazolyl) group and each of which is optionally substituted in the 5-,6-,7- or 8-position by a second carboxyl or (5-tetrazolyl) group or a substituent selected from cyano, halogen, nitro, alkyl, alkoxy, acyl, amino, acylamino, thioalkyl, alkylsulphinyl and alkylsulphonyl, as well as salts, and optionally substituted esters and amides of the carboxyl substituted compounds and alkyl derivatives of the tetrazolyl substituted compounds, are useful for the relief or prophylaxis of allergic conditions.
