52333-88-7 Usage
Description
2-Ethyloxazolo[4,5-b]pyridine is a heterocyclic chemical compound with the molecular formula C7H7NO. It features a pyridine ring fused to an oxazole ring, with an ethyl group attached to the nitrogen atom. 2-ETHYLOXAZOLO[4,5-B]PYRIDINE serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, and has been studied for its potential biological activities, such as neuroprotection. Furthermore, it has been investigated for its potential use in developing new materials and as a catalyst in organic synthesis reactions.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-Ethyloxazolo[4,5-b]pyridine is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Neuroprotective Applications:
As a neuroprotective agent, 2-ethyloxazolo[4,5-b]pyridine is studied for its potential to protect neurons from damage or degeneration, which could be beneficial in the treatment of neurological disorders.
Used in Material Science:
2-Ethyloxazolo[4,5-b]pyridine has been investigated for its potential use in the development of new materials, owing to its unique chemical structure and properties.
Used as a Catalyst in Organic Synthesis:
2-ETHYLOXAZOLO[4,5-B]PYRIDINE has also been explored for its potential as a catalyst in organic synthesis reactions, which could enhance the efficiency and selectivity of various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 52333-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,3 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52333-88:
(7*5)+(6*2)+(5*3)+(4*3)+(3*3)+(2*8)+(1*8)=107
107 % 10 = 7
So 52333-88-7 is a valid CAS Registry Number.
52333-88-7Relevant articles and documents
A green route for the synthesis of 2-substituted benzoxazole derivatives catalyzed by Al3+-exchanged K10 clay
Suresh, Dhanusu,Dhakshinamoorthy, Amarajothi,Pitchumani, Kasi
supporting information, p. 6415 - 6419 (2013/11/19)
A new, simple, and efficient protocol is developed for the synthesis of 2-substituted benzoxazole derivatives through N-C-O bond formation using Al 3+-exchanged K10 clay (Al3+-K10) as catalyst. A wide range of benzoxazole derivatives
Mild and efficient synthesis of benzoxazoles, benzothiazoles, benzimidazoles, and oxazolo[4,5-b]pyridines catalyzed by Bi(III) salts under solvent-free conditions
Mohammadpoor-Baltork, Iraj,Khosropour, Ahmad R.,Hojati, Seyedeh F.
, p. 663 - 667 (2008/02/07)
A series of benzoxazoles, benzothiazoles, benzimidazoles, and oxazolo[4,5-b]pyridines was efficiently synthesized from the reactions of o-aminophenols, o-aminothiophenol, o-phenylenediamines, and 2-amino-3- hydroxypyridine with orthoesters in the presence of catalytic amounts of Bi(III) salts, such as Bi(TFA)3, Bi(OTf)3, and BiOClO4 ? xH2O under solvent-free conditions. The remarkable features of this new protocol are high conversion, very short reaction times, cleaner reaction profiles under solvent-free conditions, straightforward procedure, and use of relatively non-toxic catalysts. Springer-Verlag 2007.
Synthesis of novel heterocycles: Oxazolo[4,5-b]pyridines and oxazolo[4,5-d]pyrimidines
Doise,Dennin,Blondeau,Sliwa
, p. 1155 - 1156 (2007/10/02)
Novel purine isosters (title compounds) have been prepared by condensation of the appropriate o-hydroxyaminoazine with ethyl orthoformate; extension to other orthoesters and to benzyl thioacetimidate afford 2-alkyl substituted derivatives of these new fus
