52904-17-3 Usage
Description
3-(trifluoromethyl)phenyl methanesulfonate is a chemical compound that features a phenyl ring with a trifluoromethyl group and a methanesulfonate group attached. It is known for its high reactivity and its ability to form new carbon-fluorine bonds through various chemical reactions.
Uses
Used in Organic Synthesis:
3-(trifluoromethyl)phenyl methanesulfonate is used as a reagent for the introduction of the trifluoromethyl group into organic molecules, which is crucial for enhancing the properties of these molecules, such as their stability and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(trifluoromethyl)phenyl methanesulfonate serves as a building block for the synthesis of various biologically active compounds. Its incorporation into these compounds can potentially improve their therapeutic effects and pharmacological properties.
Used in Agrochemical Development:
3-(trifluoromethyl)phenyl methanesulfonate has been studied for its potential use as an intermediate in the development of agrochemicals. Its unique properties may contribute to the creation of more effective and targeted agrochemicals for agricultural applications.
Used in Material Science:
Additionally, 3-(trifluoromethyl)phenyl methanesulfonate is being explored for its potential in the development of materials with specific properties. Its ability to form stable carbon-fluorine bonds can be leveraged to create materials with enhanced characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52904-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,0 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52904-17:
(7*5)+(6*2)+(5*9)+(4*0)+(3*4)+(2*1)+(1*7)=113
113 % 10 = 3
So 52904-17-3 is a valid CAS Registry Number.
52904-17-3Relevant articles and documents
Chromatography-Free and Eco-Friendly Synthesis of Aryl Tosylates and Mesylates
Lei, Xiangyang,Jalla, Anusha,Abou Shama, Mhd A.,Stafford, Jamie M.,Cao, Billy
supporting information, p. 2578 - 2585 (2015/09/01)
Two chromatography-free and eco-friendly protocols have been developed to synthesize aryl tosylates and mesylates by the tosylation and mesylation of the corresponding hydroxyarenes, respectively. These protocols are superior to other known ones regarding
A simple preparation of aryl methanesulfonates by thermal decomposition of dry arenediazonium O-benzenedisulfonimides in methanesulfonic acid
Barbero, Margherita,Degani, Iacopo,Dughera, Stefano,Fochi, Rita,Perracino, Paolo
, p. 90 - 93 (2007/10/03)
Aryl methansulfonates 3 (18 examples) were easily prepared by thermal decomposition of dry arenediazonium o-benzenedisulfonimides 1 in methanesulfonic acid (2). The reactions were carried out at temperatures between 60 and 120°C for times between 0.5 and 8 h. The aryl methanesulfonates were obtained in reproducible yield of 70-90%, with few exceptions. In all cases the o-benzenedisulfonimide (4) could be recovered in good yields which can then be reused to prepare the salts 1. When thermal decomposition of salts 1 was carried out in trifluoromethanesulfonic acid (5) at 90-120°C for 1-2 h, aryl trifluoromethanesulfonates 6 were obtained in 73-78% yield (3 examples).
