67132-84-7 Usage
Description
Cyclobutylphenylsulfide, with the molecular formula C10H12S, is a chemical compound that features a cyclobutyl group and a phenyl group connected to a sulfur atom. As a sulfide derivative, it is a versatile building block in the synthesis of a variety of sulfur-containing organic compounds. Its role extends beyond organic chemistry research, where it serves as a starting material for the preparation of more complex molecules, to potential applications in pharmaceuticals and agrochemicals due to its bioactivity.
Uses
Used in Organic Chemistry Research:
Cyclobutylphenylsulfide is used as a starting material for the synthesis of complex organic molecules, facilitating the development of novel chemical products and materials.
Used in Pharmaceutical Development:
Cyclobutylphenylsulfide is used as a potential bioactive compound in pharmaceuticals, indicating its possible role in the creation of new drugs.
Used in Agrochemicals:
In the agrochemical industry, Cyclobutylphenylsulfide is also considered for its potential applications, suggesting its use in developing new agrochemical products.
These uses underscore Cyclobutylphenylsulfide's importance in the advancement of chemical sciences and its contribution to the creation of innovative materials and compounds across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 67132-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67132-84:
(7*6)+(6*7)+(5*1)+(4*3)+(3*2)+(2*8)+(1*4)=127
127 % 10 = 7
So 67132-84-7 is a valid CAS Registry Number.
67132-84-7Relevant articles and documents
Base-Mediated Radical Borylation of Alkyl Sulfones
Huang, Mingming,Hu, Jiefeng,Krummenacher, Ivo,Friedrich, Alexandra,Braunschweig, Holger,Westcott, Stephen A.,Radius, Udo,Marder, Todd B.
supporting information, (2021/12/02)
A practical and direct method was developed for the production of versatile alkyl boronate esters via transition metal-free borylation of primary and secondary alkyl sulfones. The key to the success of the strategy is the use of bis(neopentyl glycolato) diboron (B2neop2), with a stoichiometric amount of base as a promoter. The practicality and industrial potential of this protocol are highlighted by its wide functional group tolerance, the late-stage modification of complex compounds, no need for further transesterification, and operational simplicity. Radical clock, radical trap experiments, and EPR studies were conducted which show that the borylation process involves radical intermediates.
