501120-99-6 Usage
General Description
"(R)-3-(P-Nitrophenyl)-beta-alanine is a chemical compound with a specific spatial configuration depicted by the (R) in its name, indicating its stereochemistry. The presence of a nitro group attached to a phenyl ring (P-Nitrophenyl) describes its structural feature, making it a nitroaromatic compound, which often carries unique chemical properties like having high reactivity, electron-acceptance, and more. Beta-alanine signifies it belongs to the beta amino acids family, where the amino group is at the beta-position from the carboxylate group. Overall, this chemical entity may have potential applications in creating new materials, pharmaceuticals, or agrochemical developments, primarily due to its nitroaromatic and amino acid features, although specific uses would need further explorations and confirmations.
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
