190076-45-0 Usage
Heterocyclic organic compound
The compound contains an imidazole ring, which is a heterocyclic ring system containing at least one nitrogen atom.
Imidazole ring
The central structure of the compound is a five-membered imidazole ring, which is known for its aromatic and coordinating properties.
4-Methoxyphenyl group
A phenyl group (a six-membered aromatic ring) is attached to the imidazole ring, and it has a methoxy group (-OCH3) substituting one of its hydrogen atoms.
Phenyl group
Another phenyl group is attached to the imidazole ring, which may contribute to the compound's biological activity and stability.
Oxide
The compound contains an oxygen atom bonded to the imidazole ring, which may affect its reactivity and properties.
Potential biological activities
The compound may exhibit biological activity, making it a potential candidate for pharmaceutical development or as a building block in the synthesis of biologically active molecules.
Building block in synthesis
Due to its unique structure and properties, the compound can be used as a starting material or intermediate in the synthesis of various pharmaceuticals and other biologically active molecules.
Context-dependent properties and applications
The specific properties and potential applications of the compound may vary depending on the context in which it is used, such as the target biological system or the desired therapeutic effect.
Check Digit Verification of cas no
The CAS Registry Mumber 190076-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,0,7 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 190076-45:
(8*1)+(7*9)+(6*0)+(5*0)+(4*7)+(3*6)+(2*4)+(1*5)=130
130 % 10 = 0
So 190076-45-0 is a valid CAS Registry Number.
190076-45-0Relevant academic research and scientific papers
Rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates to pyrrolo[1,2-e]imidazol-6-ols, precursors of 2,5-dihydro-1H-pyrrole derivatives
Co?kun, Necdet,?etin, Meliha
experimental part, p. 648 - 658 (2009/04/07)
Isoxazolines 2 from the cycloaddition of imidazoline 3-oxides 1 with DMAD rearrange in the presence of methoxide to give cis-3-methoxy-7-(methoxycarbonyl)-2,7a-diaryl-5-oxo-2,3,5,7a-tetrahydro-1H-pyrrolo[1,2-e]imidazol-6-olates 3 with 100% de. The acidic
A facile stereoselective synthesis of 2-perfluoroalkyl-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazoles
Lu, Lei,Cao, Weiguo,Chen, Jie,Zhang, Hui,Zhang, Jiaping,Chen, Huiyun,Wei, Jiamei,Deng, Hongmei,Shao, Min
experimental part, p. 295 - 300 (2009/12/01)
Methyl 2-perfluoroalkynoates 2 reacted readily with cyclic nitrones 1 via 1,3-dipolar cycloaddition at room temperature to give 2-perfluoroalkyl-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazoles 3 in good to excellent yields with high diastereoselectivity and r
Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates
Coskun, Necdet
, p. 13873 - 13882 (2007/10/03)
Δ3-Imidazoline 3-oxides 1 underwent regio and diastereoselective cycloaddition with aryl isocyanates 2 to give 5,6,7,7a-tetrahydroimidazo[1,5-b][1,2,4]oxadiazol-2(1H)-ones 3 in excellent yields. Thermally and chemically induced retro cycloaddit
