501120-99-6 Usage
Uses
Used in Pharmaceutical Development:
(R)-3-(P-Nitrophenyl)-beta-alanine is used as a building block or intermediate in the synthesis of pharmaceutical compounds, leveraging its nitroaromatic and amino acid features to create novel drug molecules with potential therapeutic applications.
Used in Agrochemical Research:
(R)-3-(P-Nitrophenyl)-beta-alanine is used as a chemical intermediate in the development of agrochemicals, such as pesticides or herbicides, where its unique properties may contribute to the creation of more effective and environmentally friendly products.
Used in Material Science:
(R)-3-(P-Nitrophenyl)-beta-alanine is used as a component in the design and synthesis of new materials, potentially contributing to advancements in areas like polymer chemistry, where its structural features could enhance material properties or introduce new functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 501120-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,1,2 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 501120-99:
(8*5)+(7*0)+(6*1)+(5*1)+(4*2)+(3*0)+(2*9)+(1*9)=86
86 % 10 = 6
So 501120-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O4/c10-8(5-9(12)13)6-1-3-7(4-2-6)11(14)15/h1-4,8H,5,10H2,(H,12,13)/t8-/m1/s1
501120-99-6Relevant articles and documents
Mechanism-inspired engineering of phenylalanine aminomutase for enhanced β-regioselective asymmetric amination of cinnamates
Wu, Bian,Szymanski, Wiktor,Wybenga, Gjalt G.,Heberling, Matthew M.,Bartsch, Sebastian,Dewildeman, Stefaan,Poelarends, Gerrit J.,Feringa, Ben L.,Dijkstra, Bauke W.,Janssen, Dick B.
supporting information; experimental part, p. 482 - 486 (2012/03/22)
Turn to switch: A mutant of phenylalanine aminomutase was engineered that can catalyze the regioselective amination of cinnamate derivatives (see scheme, red) to, for example, β-amino acids. This regioselectivity, along with the X-ray crystal structures, suggests two distinct carboxylate binding modes differentiated by Cβi￡Cipso bond rotation, which determines if β- (see scheme) or α-addition takes place. Copyright
Enzymatic process for the enantiomeric resolution of amino acids
-
, (2008/06/13)
An enzymatic process permitting the enantiomeric resolution of amino acids is provided. More specifically, this process for separating the enantiomers of an amino acid comprises treating a racemic mixture of the amino acid with glutaric anhydride and then with the enzyme glutaryl-7-ACA acylase so as to recover one of the enantiomers of the amino acid, the other enantiomer remaining in the form of the corresponding glutarylamide derivative.
