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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-7-carbonitrile

N#Cc1ccn2c(c1)ncc2 Request for Quotation
Chemical Name: imidazo[1,2-a]pyridine-7-carbonitrile
CAS Number: 952566-04-0
Product Number: AG00IIW9(AGN-PC-0ALTIP)
Synonyms:
MDL No:
Molecular Formula: C8H5N3
Molecular Weight: 143.1454

Identification/Properties

Computed Properties
Molecular Weight:
143.149g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
143.048g/mol
Monoisotopic Mass:
143.048g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
193
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:
Danger
UN#:
3439
Hazard Statements:
H301+H311+H331
Precautionary Statements:
P261-P280-P301+P310-P311
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Imidazo[1,2-a]pyridine-7-carbonitrile is a versatile building block in chemical synthesis due to its unique structural features and reactivity. This compound serves as a valuable intermediate in the synthesis of biologically active compounds, pharmaceuticals, and functional materials. The presence of the cyano group makes it a valuable precursor for the introduction of various functional groups through chemical transformations such as nucleophilic substitution, reduction, and metal-catalyzed reactions. Imidazo[1,2-a]pyridine-7-carbonitrile demonstrates potential in the development of novel molecules with diverse applications in medicinal chemistry, agrochemicals, and materials science. Its ability to serve as a scaffold for molecular modifications underscores its significance in synthetic organic chemistry.