73242-19-0 Usage
Uses
Used in Organic Synthesis:
2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE is used as a key intermediate in the synthesis of various organic compounds, facilitating the creation of a diverse range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE is used as an intermediate for the production of drugs, contributing to the development of new medicinal compounds.
Used in Agrochemical Production:
Similarly, in agrochemicals, 2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE serves as an intermediate, playing a crucial role in the synthesis of crop protection agents and other agricultural products.
Used in the Food Industry:
2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE is used as a flavoring agent, enhancing the taste profiles of various food products.
Used in Perfumes and Personal Care Products:
In the fragrance industry, 2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE is utilized as an ingredient in perfumes, contributing to the creation of unique scent profiles. It is also used in personal care products to add fragrance.
Used in Research and Development:
2,2-DIMETHYL-4'-THIOMETHYLPROPIOPHENONE is studied for its potential biological and pharmacological activities, such as antimicrobial and antioxidant properties, indicating its use in scientific research for new applications and therapeutic developments.
Check Digit Verification of cas no
The CAS Registry Mumber 73242-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73242-19:
(7*7)+(6*3)+(5*2)+(4*4)+(3*2)+(2*1)+(1*9)=110
110 % 10 = 0
So 73242-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H16OS/c1-12(2,3)11(13)9-5-7-10(14-4)8-6-9/h5-8H,1-4H3
73242-19-0Relevant academic research and scientific papers
N-Heterocyclic Carbene-Catalyzed Decarboxylative Alkylation of Aldehydes
Ishii, Takuya,Kakeno, Yuki,Nagao, Kazunori,Ohmiya, Hirohisa
supporting information, p. 3854 - 3858 (2019/04/25)
We found that N-heterocyclic carbene catalysis promoted the unprecedented decarboxylative coupling of aryl aldehydes and tertiary or secondary alkyl carboxylic acid-derived redox-active esters to produce aryl alkyl ketones. The mild and transition-metal-free reaction conditions are attractive features of this method. The power of this protocol was demonstrated by the functionalization of pharmaceutical drugs and natural product. A reaction pathway involving single electron transfer from an enolate form of Breslow intermediate to a redox ester followed by recombination of the resultant radical pair to form a carbon-carbon bond is proposed.
Friedel-Crafts acylation using bismuth triflate in [BMI][PF6]
Tran, Phuong Hoang,Duus, Fritz,Le, Thach Ngoc
experimental part, p. 222 - 224 (2012/01/30)
Bismuth trifluoromethanesulfonate was found to be a good catalyst for the Friedel-Crafts acylation. Bismuth triflate immobilized in an ionic liquid was the most efficient catalytic system. Bismuth triflate in [BMI][PF6] catalyzes this reaction under microwave irradiation allowing the rapid synthesis of aryl ketones in excellent yields. The catalyst system was easily recovered and reused several times.
