213701-14-5 Usage
Uses
Used in Organic Synthesis:
4-(TRIFLUOROVINYLOXYPHENYL)BORONIC ACID is used as a reagent in organic synthesis for its ability to participate in Suzuki-Miyaura coupling reactions, which are crucial for constructing carbon-carbon bonds in organic molecules. This application is vital for the creation of complex organic structures and contributes to the advancement of organic chemistry.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-(TRIFLUOROVINYLOXYPHENYL)BORONIC ACID is utilized as a building block in the development and production of various pharmaceuticals. Its role in facilitating key chemical reactions allows for the synthesis of a wide range of medicinal compounds, thereby contributing to the discovery and creation of new drugs.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 4-(TRIFLUOROVINYLOXYPHENYL)BORONIC ACID is employed as a building block for the synthesis of different agrochemicals. Its contribution to the formation of essential chemical bonds is key to the development of products that are used in agriculture to protect crops and enhance yields.
Used in Material Science:
4-(TRIFLUOROVINYLOXYPHENYL)BORONIC ACID also shows promise in the field of material science, where it is used as a tool in the development of new materials. Its unique properties and reactivity make it a valuable component in the creation of innovative materials with potential applications in various industries.
Used in Biomolecule Modification:
Furthermore, 4-(TRIFLUOROVINYLOXYPHENYL)BORONIC ACID is used as a reagent for the modification of biomolecules. This application is significant in biochemistry, as it allows for the alteration of biomolecules to study their functions, improve their properties, or develop new biological tools and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 213701-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,7,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 213701-14:
(8*2)+(7*1)+(6*3)+(5*7)+(4*0)+(3*1)+(2*1)+(1*4)=85
85 % 10 = 5
So 213701-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BF3O3/c10-7(11)8(12)15-6-3-1-5(2-4-6)9(13)14/h1-4,13-14H
213701-14-5Relevant academic research and scientific papers
Synthesis and electronic factors in thermal cyclodimerization of functionalized aromatic trifluorovinyl ethers
Spraul, Bryan K.,Suresh,Jin, Jianyong,Smith Jr., Dennis W.
, p. 7055 - 7064 (2007/10/03)
A series of 19 p-substituted aromatic trifluorovinyl ether compounds were prepared from versatile intermediate P-Br-C6H4-O-CF= CF2 and underwent thermal radical mediated cyclodimerization to new difunctional compounds cont
Synthesis of novel monomers containing the Trifluorovinylidene-group and the Cyanato-group and polymers thereof
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Page/Page column 24-25, (2010/11/24)
Novel hybrid monomers contaning both the aryltrifluorovyinyloxyether-group (TFVE-group) and the cyanato-group, their synthesis, and the synthesis of homo- and co-polymers made from these new hybridmonomers are disclosed. The said monomers are preferably of formula (III): wherein R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 can independently be selected from among a broad variety of substituents, R 11 is a single bond or is an alkylene group, R 13 and R 14 are both preferably F, and R 11 , R 15 and R 16 can be either F or H, Y and z are independent from each other and each Y and/or z can independently (in case q and/or n are more than 1) be selected from a chemical bond, SO 2 , CF 2 , CH 2 , CHF, CH(CH 3 ) 2 , isopropylene, hexafluoroisopropylene, n- or iso-C 1 -C 18 alkylene which may be partly or fully fluorinated, 0, NR 19 , N=N, CH=CH, -(C=O)-O-, -O-(C=O)-, CH=N, -C‰?C-, CHN-N=CH, alkyloxyalkylene having 1 to 18 carbon atoms which is optionally partly or fully fluorinated, S, Si(CH 3 ) 2 or wherein R 19 is hydrogen or C 1 -C 18 alkyl, Q has the same meaning as Y, m is 0 or 1, n is 0, or an integer between 1 and 6, o is 0 or an integer between 1 and 12, p is 0 or 1, and q is 0 or an integer between 1 and 6.
Synthesis of 4,6-disubstituted pyrimidines via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine
Qing, Feng-ling,Wang, Ruowen,Li, Benhan,Zheng, Xing,Meng, Wei-Dong
, p. 21 - 24 (2007/10/03)
A series of 4,6-disubstituted pyrimidines were synthesized via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine.
