2168-99-2 Usage
Uses
Used in Pharmaceutical Industry:
[(hexylsulfinyl)methyl]benzene serves as a crucial intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to participate in numerous reactions, facilitating the creation of a wide array of medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, [(hexylsulfinyl)methyl]benzene is employed as a precursor for the production of different agrochemicals. Its versatility in chemical reactions makes it a valuable component in developing compounds that cater to the needs of this industry.
Used as a Solvent:
[(hexylsulfinyl)methyl]benzene is widely used as a solvent in multiple industries due to its ability to dissolve a broad range of substances. Its solvent properties make it an indispensable component in various chemical processes and formulations.
Used in Industrial and Consumer Products:
This organic compound can also be found in some industrial and consumer products, where it plays a significant role in enhancing their performance and functionality.
Safety Precautions:
While [(hexylsulfinyl)methyl]benzene is considered to have low toxicity, it is essential to take proper safety measures when handling or working with this chemical. Exposure may cause irritation to the skin, eyes, and respiratory tract, emphasizing the need for appropriate protective equipment and handling procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 2168-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2168-99:
(6*2)+(5*1)+(4*6)+(3*8)+(2*9)+(1*9)=92
92 % 10 = 2
So 2168-99-2 is a valid CAS Registry Number.
2168-99-2Relevant academic research and scientific papers
Laccase-TEMPO as an efficient catalyst system for metal- and halogen-free aerobic oxidation of thioethers to sulfoxides in aqueous media at ambient conditions
Rostami, Amin,Mohammadi, Behnaz,Shokri, Zahra,Saadati, Shaghayegh
, p. 59 - 63 (2018/11/23)
We present for the first time an eco-friendly procedure for the aerobic oxidation of thioethers to sulfoxides using laccase-TEMPO catalyst system. This catalyst system allows for simpler (easy work-up) and greener methodologies (room temperature, phosphate buffer) while keeping high reaction yields and selectivity. This work is superior to others due to free from any transition metal and halide co-catalysts.
β-Sulfinyl acrylate esters as a convenient source of alkane- and arenesulfenate anions
O'Donnell, Jennifer S.,Schwan, Adrian L.
, p. 6293 - 6296 (2007/10/03)
Methyl acrylate esters bearing alkane- and arenesulfinyl units on the 2-carbon liberate sulfenate anions upon nucleophilic attack. The sulfenates are readily captured through sulfur alkylation. When a sulfenate derived from R-cysteine is generated, diastereoselective benzylation is observed.
