1036760-03-8 Usage
Uses
Used in Organic Synthesis:
3-(1-Hydroxyethyl)phenylboronic acid is used as a reagent in organic synthesis for its selective binding and activation of diols. Its ability to form reversible covalent bonds with certain biomolecules makes it a valuable tool in the synthesis of complex organic compounds and the development of novel chemical reactions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-(1-Hydroxyethyl)phenylboronic acid is utilized as a potential therapeutic agent, particularly in the area of diabetes treatment. Its unique chemical properties allow it to interact with specific biological targets, offering a promising avenue for the development of new drugs to manage and treat diabetes.
Used in Chemical Biology Research:
3-(1-Hydroxyethyl)phenylboronic acid is employed as a research tool in chemical biology to study the interactions between small molecules and biomolecules. Its ability to form reversible covalent bonds with certain biomolecules aids in understanding the underlying mechanisms of biological processes and contributes to the discovery of new therapeutic targets and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 1036760-03-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,6 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1036760-03:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*6)+(3*0)+(2*0)+(1*3)=128
128 % 10 = 8
So 1036760-03-8 is a valid CAS Registry Number.
InChI:InChI=1S/C8H11BO3/c1-6(10)7-3-2-4-8(5-7)9(11)12/h2-6,10-12H,1H3
1036760-03-8Relevant articles and documents
Oxidation of hydroxyl-substituted organotrifluoroborates
Molander, Gary A.,Petrillo, Daniel E.
, p. 9634 - 9635 (2006)
Potassium- and tetra-n-butylammonium organotrifluoroborates containing hydroxyl groups have been prepared and oxidized using several common oxidants. Aryl-, alkenyl-, and alkyltrifluoroborates containing both primary and secondary hydroxyl groups were oxi
Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols
Andrade, Leandro H.,Barcellos, Thiago
supporting information; experimental part, p. 3052 - 3055 (2009/12/05)
The first application of enzymes as catalysts to obtain optically pure boron compounds is described. The kinetic resolution of boron-containing chiral alcohols via enantioselective transesterification catalyzed by lipases was studied. Aromatic, allylic, and aliphatic secondary alcohols containing a boronate ester or boronic acid group were resolved by lipase from Candida antartica (CALB), and excellent E values (E > 200) and high enantiomeric excesses (up to >99%) of both remaining substrates and acetylated product were obtained.
