232275-88-6 Usage
Description
(2,6-bis(methoxymethoxy)phenyl)boronic acid is a boronic acid derivative with the molecular formula C12H17BO6. It features a phenyl ring with two methoxymethoxy groups attached, making it a versatile building block in organic and medicinal chemistry.
Uses
Used in Organic Synthesis:
(2,6-bis(methoxymethoxy)phenyl)boronic acid is used as a building block for the synthesis of various organic compounds. Its ability to react with diols and other nucleophiles makes it a valuable component in creating complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (2,6-bis(methoxymethoxy)phenyl)boronic acid is used as a key intermediate in the development of new drugs. Its reactivity and structural features contribute to the creation of potential therapeutic agents.
Used in Materials Science:
(2,6-bis(methoxymethoxy)phenyl)boronic acid is utilized in the field of materials science to develop new materials with specific properties. Its incorporation into material structures can lead to advancements in areas such as polymers, coatings, and composites.
Used as a Reagent in Chemical Reactions:
In the realm of chemical reactions, (2,6-bis(methoxymethoxy)phenyl)boronic acid serves as a reagent, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful method for forming carbon-carbon bonds, which is essential in the synthesis of many organic compounds.
Overall, (2,6-bis(methoxymethoxy)phenyl)boronic acid is a multifaceted compound with applications spanning across various industries, highlighting its importance in modern chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 232275-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,2,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 232275-88:
(8*2)+(7*3)+(6*2)+(5*2)+(4*7)+(3*5)+(2*8)+(1*8)=126
126 % 10 = 6
So 232275-88-6 is a valid CAS Registry Number.
232275-88-6Relevant articles and documents
Competitive Binding Assay with an Umbelliferone-Based Fluorescent Rexinoid for Retinoid X Receptor Ligand Screening
Yamada, Shoya,Kawasaki, Mayu,Fujihara, Michiko,Watanabe, Masaki,Takamura, Yuta,Takioku, Maho,Nishioka, Hiromi,Takeuchi, Yasuo,Makishima, Makoto,Motoyama, Tomoharu,Ito, Sohei,Tokiwa, Hiroaki,Nakano, Shogo,Kakuta, Hiroki
, p. 8809 - 8818 (2019/10/11)
Ligands for retinoid X receptors (RXRs), "rexinoids", are attracting interest as candidates for therapy of type 2 diabetes and Alzheimer's and Parkinson's diseases. However, current screening methods for rexinoids are slow and require special apparatus or facilities. Here, we created 7-hydroxy-2-oxo-6-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-2H-chromene-3-carboxylic acid (10, CU-6PMN) as a new fluorescent RXR agonist and developed a screening system of rexinoids using 10. Compound 10 was designed based on the fact that umbelliferone emits strong fluorescence in a hydrophilic environment, but the fluorescence intensity decreases in hydrophobic environments such as the interior of proteins. The developed assay using 10 enabled screening of rexinoids to be performed easily within a few hours by monitoring changes of fluorescence intensity with widely available fluorescence microplate readers, without the need for processes such as filtration.
Facile and highly enantioselective synthesis of axially chiral biaryls by enzymatic desymmetrization
Matsumoto,Konegawa,Nakamura,Suzuki
, p. 122 - 124 (2007/10/03)
The axially chiral biaryls 2 were obtained in high enantioselectivity by desymmetrization of the σ-symmetric biaryl diacetates 1 by lipase-catalyzed hydrolysis.
