2070902-77-9 Usage
Uses
Used in Organic Synthesis:
Trifluoromethyl 4-fluorobenzene-1-sulfonate is utilized as a building block in organic synthesis for its ability to enhance the properties of organic molecules. It is particularly valuable for its role in creating new compounds with improved characteristics.
Used in Pharmaceutical Research:
In pharmaceutical research, trifluoromethyl 4-fluorobenzene-1-sulfonate is employed as a reagent for introducing the trifluoromethyl group into organic molecules. This modification can lead to the development of novel pharmaceuticals with potentially enhanced efficacy and selectivity.
Used in Material Development:
trifluoromethyl 4-fluorobenzene-1-sulfonate is also used in the development of new materials, where its unique properties can contribute to the creation of innovative products with specific applications.
Safety Considerations:
It is crucial to handle trifluoromethyl 4-fluorobenzene-1-sulfonate with care and to follow proper safety procedures. trifluoromethyl 4-fluorobenzene-1-sulfonate can react violently in the presence of strong oxidizing agents, necessitating caution during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2070902-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,7,0,9,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2070902-77:
(9*2)+(8*0)+(7*7)+(6*0)+(5*9)+(4*0)+(3*2)+(2*7)+(1*7)=139
139 % 10 = 9
So 2070902-77-9 is a valid CAS Registry Number.
2070902-77-9Relevant academic research and scientific papers
Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates
Yang, Yu-Ming,Yao, Jian-Fei,Yan, Wei,Luo, Zhuangzhu,Tang, Zhen-Yu
supporting information, p. 8003 - 8007 (2019/10/11)
Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds.
Bromotrifluoromethoxy compound and synthetic method thereof
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Paragraph 0061; 0062; 0064; 0065, (2017/08/27)
According to the invention, a series of trifluoromethoxy reagent precursors are synthesized, and trifluoromethoxy silver with high activity can be obtained under the condition of an activating reagent. By the utilization of the idea, a bromotrifluorometho
