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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-3-carboxylic acid, 2-methyl-, ethyl ester

CCOC(=O)c1c(C)nc2n1cccc2 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl-, ethyl ester
CAS Number: 2549-19-1
Product Number: AG00BCUL(AGN-PC-0JVSC4)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O2
Molecular Weight: 204.2252

Identification/Properties

Computed Properties
Molecular Weight:
204.229g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
204.09g/mol
Monoisotopic Mass:
204.09g/mol
Topological Polar Surface Area:
43.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
245
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-methylimidazo[1,2-a]pyridine-3-carboxylate is a versatile compound commonly utilized in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound is particularly valuable in medicinal chemistry for its role in the development of novel drug molecules with potential therapeutic applications. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic compounds, enabling chemists to access diverse chemical functionalities and molecular architectures. In addition, Ethyl 2-methylimidazo[1,2-a]pyridine-3-carboxylate serves as a valuable tool in the study of structure-activity relationships and the exploration of new chemical reactions. Its incorporation into synthetic routes allows for the efficient preparation of diverse chemical libraries, facilitating the discovery of new bioactive compounds and enabling the advancement of drug discovery efforts.