90717-66-1 Usage
Uses
Used in Pharmaceutical Development:
3-(3-AMINO-4-HYDROXY-PHENYL)-PROPIONIC ACID is utilized as a precursor in the development of new drugs due to its potential antioxidant and anti-inflammatory properties. These characteristics make it a candidate for treating a variety of diseases where oxidative stress and inflammation are contributing factors.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-(3-AMINO-4-HYDROXY-PHENYL)-PROPIONIC ACID is used as a subject of study for its potential to interact with specific receptors and enzymes. This interaction could lead to the discovery of novel mechanisms of action for treating diseases and the creation of more effective therapeutic agents.
Used in Drug Discovery:
3-(3-AMINO-4-HYDROXY-PHENYL)-PROPIONIC ACID is employed as a compound of interest in drug discovery efforts. Its unique structure and functional groups may contribute to the development of innovative drugs that target particular biological pathways or processes, offering new treatment options for patients.
Check Digit Verification of cas no
The CAS Registry Mumber 90717-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90717-66:
(7*9)+(6*0)+(5*7)+(4*1)+(3*7)+(2*6)+(1*6)=141
141 % 10 = 1
So 90717-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c10-7-5-6(1-3-8(7)11)2-4-9(12)13/h1,3,5,11H,2,4,10H2,(H,12,13)
90717-66-1Relevant articles and documents
Synthesis of Benzoxazoles Using Electrochemically Generated Hypervalent Iodine
Koleda, Olesja,Broese, Timo,Noetzel, Jan,Roemelt, Michael,Suna, Edgars,Francke, Robert
, p. 11669 - 11681 (2017/11/24)
The indirect ("ex-cell") electrochemical synthesis of benzoxazoles from imines using a redox mediator based on the iodine(I)/iodine(III) redox couple is reported. Tethering the redox-active iodophenyl subunit to a tetra-alkylammonium moiety allowed for anodic oxidation to be performed without supporting electrolyte. The mediator salt can be easily recovered and reused. Our "ex-cell" approach toward the electrosynthesis of benzoxazoles is compatible with a range of redox-sensitive functional groups. An unprecedented concerted reductive elimination mechanism for benzoxazole formation is proposed on the basis of control experiments and DFT calculations.
Photoactivated bioconjugation between ortho -azidophenols and anilines: A facile approach to biomolecular photopatterning
El Muslemany, Kareem M.,Twite, Amy A.,Elsohly, Adel M.,Obermeyer, Allie C.,Mathies, Richard A.,Francis, Matthew B.
, p. 12600 - 12606 (2014/12/11)
Methods for the surface patterning of small molecules and biomolecules can yield useful platforms for drug screening, synthetic biology applications, diagnostics, and the immobilization of live cells. However, new techniques are needed to achieve the ease
