67132-84-7 Usage
General Description
Cyclobutylphenylsulfide is a chemical compound with the molecular formula C10H12S. It is a sulfide derivative, consisting of a cyclobutyl group and a phenyl group attached to a sulfur atom. Cyclobutylphenylsulfide is often used as a building block in the synthesis of various sulfur-containing organic compounds. It is commonly employed in organic chemistry research as a starting material for the preparation of more complex molecules. Additionally, cyclobutylphenylsulfide has been implicated in several studies as a potential bioactive compound with potential applications in pharmaceuticals and agrochemicals. Overall, this compound plays a significant role in the development of novel materials and chemical products.
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.
