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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Imidazo[1,2-a]pyridine-8-carboxylic acid, methyl ester

COC(=O)c1cccn2c1ncc2 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyridine-8-carboxylic acid, methyl ester
CAS Number: 133427-07-3
Product Number: AG0080HP(AGN-PC-003QPX)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O2
Molecular Weight: 176.1720

Identification/Properties

Computed Properties
Molecular Weight:
176.175g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
176.059g/mol
Monoisotopic Mass:
176.059g/mol
Topological Polar Surface Area:
43.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
208
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl imidazo[1,2-a]pyridine-8-carboxylate, a versatile compound widely utilized in chemical synthesis, serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structural properties make it an indispensable intermediate in the synthesis of biologically active compounds, particularly in the development of novel drugs and crop protection agents.In chemical synthesis, Methyl imidazo[1,2-a]pyridine-8-carboxylate acts as a valuable precursor for the assembly of more complex molecular structures through numerous synthetic transformations such as functional group interconversions, cross-coupling reactions, and heterocycle formations. Its presence in organic synthesis pathways enables the production of diverse compounds with tailored physicochemical properties and biological activities.Moreover, the strategic incorporation of Methyl imidazo[1,2-a]pyridine-8-carboxylate into synthetic routes allows for the efficient construction of molecular scaffolds with high structural diversity, which is essential for the discovery and optimization of lead compounds in drug development and agricultural chemistry. By leveraging its synthetic utility, researchers and chemists can expedite the synthesis of target molecules with enhanced potency, selectivity, and bioavailability, thus driving innovation in the field of chemical science and promoting the advancement of various industries.