342636-66-2 Usage
Description
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is a boronic acid derivative with the molecular formula C8H10BFO2. It features a boron atom bonded to a fluorine and a phenyl group, with two methyl groups at the 3rd and 5th positions on the phenyl ring. This chemical compound is known for its versatile applications in various fields, including organic synthesis, pharmaceuticals, agrochemicals, advanced materials, and as a catalyst in chemical reactions. Furthermore, it has been investigated for its potential biological activities, such as its role as an anti-cancer agent and a component of fluorescent probes.
Uses
Used in Organic Synthesis:
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is used as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure allows for the formation of new compounds with potential therapeutic and pesticidal properties.
Used in Advanced Materials:
In the field of materials science, 3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is employed in the development of advanced materials with specific properties, such as optical, electronic, or catalytic functions. Its incorporation into these materials can enhance their performance and expand their applications.
Used as a Catalyst:
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID serves as a catalyst in various chemical reactions, promoting the formation of desired products with improved efficiency and selectivity. Its catalytic properties can be harnessed in a wide range of industrial processes, contributing to the synthesis of valuable compounds.
Used in Pharmaceutical Industry:
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity enable the development of new drugs with improved therapeutic profiles and targeted effects.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is utilized as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can lead to enhanced efficacy and selectivity, reducing the environmental impact of agricultural practices.
Used in Anti-Cancer Research:
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID has been studied for its potential as an anti-cancer agent. Its biological activities are being investigated for its ability to target and inhibit the growth of cancer cells, offering a promising avenue for the development of novel cancer therapies.
Used in Fluorescent Probes:
3,5-DIMETHYL-4-FLUORO-PHENYLBORONIC ACID is also used as a component of fluorescent probes, which are essential tools in biological and chemical research. Its incorporation into these probes can enhance their sensitivity and specificity, allowing for the detection and analysis of various biological processes and molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 342636-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 342636-66:
(8*3)+(7*4)+(6*2)+(5*6)+(4*3)+(3*6)+(2*6)+(1*6)=142
142 % 10 = 2
So 342636-66-2 is a valid CAS Registry Number.
342636-66-2Relevant articles and documents
Controlling Singlet–Triplet Energy Splitting for Deep-Blue Thermally Activated Delayed Fluorescence Emitters
Cui, Lin-Song,Nomura, Hiroko,Geng, Yan,Kim, Jong U.k.,Nakanotani, Hajime,Adachi, Chihaya
supporting information, p. 1571 - 1575 (2017/02/05)
The development of efficient metal-free organic emitters with thermally activated delayed fluorescence (TADF) properties for deep-blue emission is still challenging. A new family of deep-blue TADF emitters based on a donor–acceptor architecture has been developed. The electronic interaction between donor and acceptor plays a key role in the TADF mechanism. Deep-blue OLEDs fabricated with these TADF emitters achieved high external quantum efficiencies over 19.2 % with CIE coordinates of (0.148, 0.098).
