6-bromo-2-methylimidazo[1,2-a]pyridine-3-carbaldehyde


Chemical Name: 6-bromo-2-methylimidazo[1,2-a]pyridine-3-carbaldehyde
CAS Number: 728864-58-2
Product Number: AG005O15(AGN-PC-0KKLHO)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2O
Molecular Weight: 239.0687

Identification/Properties


Computed Properties
Molecular Weight:
239.072g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
237.974g/mol
Monoisotopic Mass:
237.974g/mol
Topological Polar Surface Area:
34.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
212
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Bromo-2-methylimidazo[1,2-a]pyridine-3-carbaldehyde is a versatile chemical intermediate commonly used in chemical synthesis processes. It serves as a key building block in the creation of various functional molecules due to its unique structure and reactivity. In organic synthesis, this compound is often employed as a key starting material for the preparation of complex pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of 6-Bromo-2-methylimidazo[1,2-a]pyridine-3-carbaldehyde is in the synthesis of heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. This aldehyde derivative undergoes various chemical reactions, such as cross-coupling reactions, cyclization reactions, and functional group transformations, to generate novel compounds with diverse properties and functionalities. By incorporating this compound into synthetic pathways, chemists can access a wide range of molecular structures that exhibit potential pharmacological, biological, or material science applications.Overall, the strategic utilization of 6-Bromo-2-methylimidazo[1,2-a]pyridine-3-carbaldehyde in chemical synthesis enables the efficient construction of complex molecules with tailored structures and properties, making it an indispensable tool for organic chemists working in drug discovery, materials science, and other research areas.