3672-37-5 Usage
Description
3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine is a member of the imidazopyridine class, specifically characterized by the presence of a phenyl group at position 2 and a nitroso group at position 3. 3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine is a derivative of imidazo[1,2-a]pyridine, which is a fused heterocyclic compound consisting of an imidazole and a pyridine ring.
Uses
Used in Pharmaceutical Industry:
3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure with phenyl and nitroso substitutions provides a versatile platform for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine serves as a valuable compound for studying the properties and reactivity of imidazopyridine derivatives. Its synthesis and functionalization can provide insights into the design and development of novel heterocyclic compounds with diverse applications.
Used in Material Science:
3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine may also find applications in material science, particularly in the development of new materials with specific optical, electronic, or magnetic properties. 3-Nitroso-2-phenyl-imidazo[1,2-a]pyridine's structural features can be exploited to create novel materials with tailored characteristics for various technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3672-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3672-37:
(6*3)+(5*6)+(4*7)+(3*2)+(2*3)+(1*7)=95
95 % 10 = 5
So 3672-37-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3O/c17-15-13-12(10-6-2-1-3-7-10)14-11-8-4-5-9-16(11)13/h1-9H
3672-37-5Relevant articles and documents
Difluorinative-hydroxylation and C-3 functionalization (halogenation/SCN/NO) of imidazopyridine using Selectfluor as fluorine source or oxidant respectively
Balasubramanian, Sridhar,Kalari, Saradhi,Rode, Haridas B.
supporting information, (2021/04/15)
An efficient route for the difluorinative-hydroxylation through dearomative difunctionalization of imidazopyridine using Selectfluor as fluorine source has been developed in an aqueous medium. The reaction proceeds through ionic followed by radical pathwa
Design and Synthesis of Imidazo[1,2-a]pyridines with Carboxamide Group Substitution and In silico Evaluation of their Interaction with a LuxR-type Quorum Sensing Receptor
Reynoso Lara, Juan Emmanuel,Salgado-Zamora, Héctor,Bazin, Marc-Antoine,Campos-Aldrete, María Elena,Marchand, Pascal
, p. 1101 - 1111 (2018/03/29)
Quorum sensing, an important process of bacterial communication, is involved in the development of complex behavior and expression of virulence factors that become important due to its key role in infection process. In this manuscript, docking studies wer
NaNO2/I2-Mediated Regioselective Synthesis of Nitrosoimidazoheterocycles from Acetophenones by a Domino Process
Mukhopadhyay, Sushobhan,Dighe, Shashikant U.,Kolle, Shivalinga,Shukla, Praveen K.,Batra, Sanjay
, p. 3836 - 3844 (2016/08/16)
A regioselective synthesis of nitrosoimidazoheterocycles from the reaction of 2-aminopyridines and acetophenones in the presence of NaNO2and I2is described. The reaction is suggested to proceed by a domino process involving sequentia
