10250-66-5 Usage
Uses
Used in Pharmaceutical Industry:
3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds for its versatile reactivity and potential biological activity. It plays a crucial role in the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and potential biological activity enable the creation of effective and environmentally friendly solutions for agricultural applications.
Used in Material Science:
3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID may have potential applications in the development of new materials due to its unique chemical structure and properties. It can be used as a component in the synthesis of advanced materials with specific characteristics, such as improved mechanical strength or thermal stability.
Used in Organic Electronics:
3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID also has potential uses in the field of organic electronics, where it can be employed in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic solar cells. Its unique properties may contribute to enhanced device performance and efficiency.
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 academic research and scientific papers
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).
NITROSATION OF N'-SUBSTITUTED 3- AND 4-UREIDOALKANOIC ACIDS
Lutsenko, V. V.,Klimavichyus, K.-A. V.
, p. 1905 - 1908 (2007/10/02)
The nitrosation of N'-substituted 3- and 4-ureidoalkanoic acids, synthesized by the condensation of 3- and 4-aminoalkanoic acids with hexyl- and phenyl isocyanates, was studied under various conditions.The ratios of the obtained N- and N'-nitroso derivatives were established by PMR spectroscopy.
