18800-53-8 Usage
Uses
Used in Chemical Synthesis Studies:
3,4-Dimethylthiophenol is used as a key intermediate in the synthesis of various organic compounds, particularly those involving thiophene rings. Its unique structure allows for a range of chemical reactions, making it a valuable building block in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Flavor and Fragrance Industry:
3,4-Dimethylthiophenol is used as a flavoring agent in the food and beverage industry, where it contributes to the characteristic taste and aroma of certain products. Its distinct sulfury note can be used to enhance the flavor profile of various dishes and beverages, adding depth and complexity to their taste.
Used in Pharmaceutical Industry:
3,4-Dimethylthiophenol is used as a starting material in the synthesis of various pharmaceutical compounds, including drugs with antibacterial, antifungal, and antiviral properties. Its unique chemical structure allows for the development of novel therapeutic agents that can target specific biological pathways and mechanisms.
Used in Material Science:
3,4-Dimethylthiophenol can be utilized in the development of advanced materials, such as conductive polymers and sensors, due to its electronic and optical properties. Its sulfur-containing structure can be exploited to create materials with enhanced electrical conductivity, making it a promising candidate for applications in electronics and energy storage.
Check Digit Verification of cas no
The CAS Registry Mumber 18800-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18800-53:
(7*1)+(6*8)+(5*8)+(4*0)+(3*0)+(2*5)+(1*3)=108
108 % 10 = 8
So 18800-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10S/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3/p-1
18800-53-8Relevant academic research and scientific papers
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.
The Synthesis of All of the Dimethyldibenzothiophenes and Monoethyldibenzothiophenes
Tedjamulia, Marvin L.,Tominaga, Yoshinori,Castle, Raymond N.
, p. 1485 - 1495 (2007/10/02)
The synthesis of all four isomers of the monoethyldibenzothiophenes and all of the sixteen isomers of the dimethyldibenzothiophenes has been accomplished.
Substituted 2-phenyl-1,2,4-triazine-3,5(2H,4H)-diones, and coccidiostatic agents containing same
-
, (2008/06/13)
Novel substituted 2-phenyl-1,2,4-triazine-3,5-(2H,4H)-diones are described as well as a process for their manufacture. The novel compounds may be used as chemotherapeutics, especially as coccidiostatic agents.
