1772625-41-8 Usage
Description
(S)-4-benzyl-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole is a heterocyclic compound characterized by the fusion of an oxazole ring with a naphthyridine moiety. This molecule features a benzyl group and a 1,8-naphthyridin-2-yl group attached to the oxazole ring, and it is classified as a chiral compound due to the presence of an asymmetric carbon atom, which leads to two possible enantiomeric forms. Its unique structure and potential biological activities suggest that it may have applications in the development of pharmaceuticals, agrochemicals, and materials. Further research is required to fully understand its pharmacological properties and explore its potential uses across different fields.
Uses
Used in Pharmaceutical Development:
(S)-4-benzyl-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole is used as a key intermediate in the synthesis of pharmaceuticals for [application reason]. Its unique structure may allow for the development of novel drugs with specific targeting capabilities or improved pharmacokinetic profiles.
Used in Agrochemicals:
In the agrochemical industry, (S)-4-benzyl-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole is used as a building block for the creation of new pesticides or herbicides for [application reason]. Its structural features may contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Materials Science:
(S)-4-benzyl-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole is utilized as a component in the development of advanced materials for [application reason]. Its incorporation into material formulations could lead to the creation of materials with enhanced properties, such as improved stability, reactivity, or selectivity in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1772625-41-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,7,2,6,2 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1772625-41:
(9*1)+(8*7)+(7*7)+(6*2)+(5*6)+(4*2)+(3*5)+(2*4)+(1*1)=188
188 % 10 = 8
So 1772625-41-8 is a valid CAS Registry Number.
1772625-41-8Relevant articles and documents
Chiral 1,8-naphthyridine based ligands: Syntheses and characterization of Di- and tetranuclear copper (I) and silver (I) complexes
Sarkar, Mithun,Pandey, Pragati,Bera, Jitendra K.
, p. 518 - 528 (2019)
Oxazoline and camphor-pyrazole units are introduced on the 1,8-naphthyridine scaffold to access chiral ligands L1, L2 and L3. Metalation of these chiral ligands with Cu(I) and Ag(I) precursors afforded di- and tetranuclear complexes [Cu4I4(L1)2] (1), [Cu4I4(L2)2] (2), [Cu2I2(L3)] (3), [Cu2I(L2)2](OTf) (4), [Ag2(L1)2](OTf)2 (5) and [Ag4(L2)4Br](OTf)3 (6), containing [M4Xn] (n = 1,4 and X = Br, I) or [M2Xn] (n = 0, 1, 2 and X = I) core. All complexes are structurally characterized. Naphthyridine-derived ligands reveal bridge-chelate coordination motif and hold two metal centers in close proximity. The tetranuclear complexes are dimer of dinuclear complexes bridged by the halides. Electronic absorption and emission spectra of copper complexes are reported. Catalytic utility of all complexes are examined for asymmetric transformations but they showed poor activity probably due to limited solubility and coordinative saturation at the metal centers. The best results are obtained with [L3/Cu salt] combination for cyclopropanation of styrene, N–H bond insertion and nitroaldol (Henry) reactions with very low enantioselectivity.
