Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methyl-


Chemical Name: Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methyl-
CAS Number: 14714-22-8
Product Number: AG001ENQ(AGN-PC-0NKLSF)
Synonyms:
MDL No:
Molecular Formula: C8H6ClN3O2
Molecular Weight: 211.6051

Identification/Properties


Computed Properties
Molecular Weight:
211.605g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
211.015g/mol
Monoisotopic Mass:
211.015g/mol
Topological Polar Surface Area:
67.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
251
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Chloro-2-methylimidazo[1,2-b]pyridazine-3-carboxylic acid is a versatile compound widely utilized in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the creation of various organic molecules. In organic synthesis, it can be employed as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. Its presence enables the introduction of specific functional groups and structural motifs into target compounds, enhancing the overall synthetic efficiency and diversity of the final products. Additionally, the distinct properties of 6-Chloro-2-methylimidazo[1,2-b]pyridazine-3-carboxylic acid make it a valuable tool for the development of novel chemical entities with potential applications in medicinal chemistry, materials science, and other fields.