10250-66-5 Usage
General Description
3-[(anilinocarbonyl)amino]propanoic acid is a chemical compound with the molecular formula C11H13NO4. It is a carboxylic acid derivative with an anilino group and a carbonyl group attached to a propanoic acid moiety. 3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and potential biological activity. It may also have potential applications in the development of new materials and organic electronic devices. However, its precise properties and uses may vary depending on its specific application and chemical context.
Check Digit Verification of cas no
The CAS Registry Mumber 10250-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10250-66:
(7*1)+(6*0)+(5*2)+(4*5)+(3*0)+(2*6)+(1*6)=55
55 % 10 = 5
So 10250-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O3/c13-9(14)6-7-11-10(15)12-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,13,14)(H2,11,12,15)/p-1
10250-66-5Relevant articles and documents
SupraBox: Chiral supramolecular oxazoline ligands
Durini, Marco,Russotto, Eleonora,Pignataro, Luca,Reiser, Oliver,Piarulli, Umberto
, p. 5451 - 5461 (2012/10/30)
A new class of oxazoline ligands, named SupraBox, was studied. These ligands possess an additional urea functionality to generate supramolecular bidentate ligands in transition-metal complexes, by the establishment of hydrogen bonds between the urea N-hydrogens of one ligand and the carbonyl oxygen of a second one. A library of 16 SupraBox ligands was prepared using 5 differently substituted oxazoline nuclei, 4 linkers and 3 different urea substituents. The formation of copper(II) and palladium(II) complexes was investigated by MS, UV/Vis and 1H-NMR spectroscopy. The SupraBox library was screened in the copper-catalyzed asymmetric benzoylation of vic-diols. Good selectivities were obtained in the kinetic resolution of racemic hydrobenzoin [up to 86 % ee and selectivity (s) = 28] and in the desymmetrization of meso-hydrobenzoin (up to 88 % ee).
