CAS 4532-25-6
:7-Chloroimidazo[1,2-a]pyridine
Description:
7-Chloroimidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, with a chlorine substituent at the 7-position of the imidazole ring. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, but has limited solubility in water. It is known for its potential biological activities, including antimicrobial and anticancer properties, making it of interest in pharmaceutical research. The presence of the chlorine atom enhances its reactivity and can influence its interaction with biological targets. Additionally, 7-Chloroimidazo[1,2-a]pyridine can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Safety data indicates that, like many chemical compounds, it should be handled with care, using appropriate safety measures to avoid exposure. Overall, this compound represents a significant structure in medicinal chemistry and material science.
Formula:C7H5ClN2
InChI:InChI=1/C7H5ClN2/c8-6-1-3-10-4-2-9-7(10)5-6/h1-5H
SMILES:c1cn2ccnc2cc1Cl
Synonyms:- 7-Chloro-imidazo[1,2-a]pyridine
- Imidazo[1,2-A]Pyridine, 7-Chloro-
- 7-chloroimidazo[1,2-α]pyridine
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Found 4 products.
7-Chloroimidazo[1,2-A]Pyridine
CAS:Formula:C7H5ClN2Purity:97%Color and Shape:SolidMolecular weight:152.58107-Chloroimidazo[1,2-a]pyridine
CAS:7-Chloroimidazo[1,2-a]pyridinePurity:98%Color and Shape:Brown SolidMolecular weight:152.58g/mol7-Chloroimidazo[1,2-a]pyridine
CAS:<p>7-Chloroimidazo[1,2-a]pyridine is a chemical compound with the molecular formula C6H4ClN. It is an aromatic heterocycle and contains a pyridine ring fused to a benzene ring. This compound has resonance between the N atom in the pyridine ring and the C atom in the imidazole ring. The proton magnetic resonance spectrum of 7-chloroimidazo[1,2-a]pyridine displays two peaks at δ H 8.5 and δ H 8.8 that correspond to the two tautomeric forms of this compound. The laboratory synthesis of 7-chloroimidazo[1,2-a]pyridine requires bromoacetaldehyde as starting material. Bromination by bromine produces 2-amino-4-chloropyridine, which reacts with acetic anhydride to form 7-chloroim</p>Formula:C7H5ClN2Purity:Min. 95%Color and Shape:PowderMolecular weight:152.58 g/mol7-Chloroimidazo[1,2-a]pyridine
CAS:Formula:C7H5ClN2Purity:97%Color and Shape:SolidMolecular weight:152.58



