436853-63-3 Usage
Explanation
A boronic acid derivative is a compound that contains a boron atom bonded to a hydroxyl group (OH) and an organic group. In this case, the organic group is a 3,5-dimethylphenyl group.
Explanation
The structure of 1,3,2-Dioxaborinane, 2-(3,5-dimethylphenyl)consists of a boron atom connected to two oxygen atoms, forming a three-membered ring, and a phenyl group attached to one of the oxygen atoms.
4. Used as a reagent in organic synthesis
Explanation
1,3,2-Dioxaborinane, 2-(3,5-dimethylphenyl)- is commonly used as a reagent in various organic synthesis reactions due to its unique properties and reactivity.
5. Utilized in Suzuki coupling reactions
Explanation
Suzuki coupling is a carbon-carbon bond-forming reaction between an organoboron compound and an organic halide or triflate in the presence of a palladium catalyst. 1,3,2-Dioxaborinane, 2-(3,5-dimethylphenyl)is often used as the organoboron compound in these reactions.
6. Applications in pharmaceuticals and agrochemicals synthesis
Explanation
Due to its reactivity and ability to form carbon-carbon bonds, 1,3,2-Dioxaborinane, 2-(3,5-dimethylphenyl)- is used in the synthesis of various pharmaceuticals and agrochemicals, which are essential for the development of new drugs and pesticides.
7. Important intermediate in organic chemistry
Explanation
As a versatile reagent with various applications, 1,3,2-Dioxaborinane, 2-(3,5-dimethylphenyl)serves as an important intermediate in the production of a wide range of chemical compounds.
Structure
Boron atom bonded to two oxygen atoms and a phenyl group
Check Digit Verification of cas no
The CAS Registry Mumber 436853-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,8,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 436853-63:
(8*4)+(7*3)+(6*6)+(5*8)+(4*5)+(3*3)+(2*6)+(1*3)=173
173 % 10 = 3
So 436853-63-3 is a valid CAS Registry Number.
436853-63-3Relevant academic research and scientific papers
Optical glucose detection across the visible spectrum using anionic fluorescent dyes and a viologen quencher in a two-component saccharide sensing system
Cordes, David B.,Miller, Aaron,Gamsey, Soya,Sharrett, Zach,Thoniyot, Praveen,Wessling, Ritchie,Singaram, Bakthan
, p. 1708 - 1713 (2007/10/03)
A very general system is described in which anionic fluorescent dyes possessing a wide range of absorbance and emission wavelengths are used in combination with a boronic acid-modified viologen quencher to sense glucose at pH 7.4 in buffered aqueous solut
Continuous Glucose Sensing with a Fluorescent Thin-Film Hydrogel
Suri, Jeff T.,Cordes, David B.,Cappuccio, Frank E.,Wessling, Ritchie A.,Singaram, Bakthan
, p. 5857 - 5859 (2007/10/03)
Sweetness and light: A fluorescent thin-film hydrogel that contains a covalently bound boronic-acid-functional quencher (Q) and a fluorescent dye (F; see Figure) continuously senses glucose under physiological conditions through binding of the sugar (S) to a labeled receptor (R).
