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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, 5-methyl-

Cc1cccc2n1ccn2 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyridine, 5-methyl-
CAS Number: 933-69-7
Product Number: AG006G7V(AGN-PC-0JMP24)
Synonyms:
MDL No:
Molecular Formula: C8H8N2
Molecular Weight: 132.1625

Identification/Properties

Properties
BP:
96°C/0.7mm
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
132.166g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
132.069g/mol
Monoisotopic Mass:
132.069g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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:
H317
Precautionary Statements:
P261-P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methylimidazo[1,2-a]pyridine, or $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and diverse applications. This heterocyclic compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials with valuable properties.In organic synthesis, 5-Methylimidazo[1,2-a]pyridine acts as a valuable intermediate in the construction of complex organic molecules due to its reactivity and structural features. It can participate in a range of chemical reactions such as substitution, oxidation, and nitration, enabling the synthesis of structurally diverse compounds.One of the prominent applications of 5-Methylimidazo[1,2-a]pyridine is in medicinal chemistry, where it is utilized as a core structure in the design and development of pharmaceutical compounds. Its presence in drug molecules imparts specific biological activities, making it a crucial component in the synthesis of drugs targeting various diseases.Furthermore, in the field of agrochemistry, 5-Methylimidazo[1,2-a]pyridine serves as a vital component in the synthesis of pesticides, herbicides, and fungicides. Its inclusion in agrochemical formulations enhances the efficacy and specificity of these compounds, contributing to sustainable crop protection and pest management practices.Additionally, 5-Methylimidazo[1,2-a]pyridine finds applications in material science, where it is incorporated into the synthesis of advanced materials with specialized properties. Its unique chemical structure and reactivity enable the creation of materials with enhanced electrical, optical, or catalytic properties, thereby expanding the scope of materials research and development.Overall, the versatility and utility of 5-Methylimidazo[1,2-a]pyridine in chemical synthesis make it a valuable compound in various industries, driving innovation and advancement in drug discovery, agriculture, and materials science.