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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)-

3-iodoimidazo[1,2-a]pyridine-6-carbonitrile

Ic1cnc2n1cc(cc2)C#N Request for Quotation
Chemical Name: 3-iodoimidazo[1,2-a]pyridine-6-carbonitrile
CAS Number: 885276-13-1
Product Number: AG0047EF(AGN-PC-0BSCDA)
Synonyms:
MDL No:
Molecular Formula: C8H4IN3
Molecular Weight: 269.0419

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
269.045g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
268.945g/mol
Monoisotopic Mass:
268.945g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
222
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Iodoimidazo[1,2-a]pyridine-6-carbonitrile is a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound serves as a key intermediate in the development of various pharmaceuticals, agrochemicals, and advanced materials. Its ability to serve as a precursor for the synthesis of heterocyclic compounds makes it valuable in medicinal chemistry for drug discovery and development. Additionally, 3-Iodoimidazo[1,2-a]pyridine-6-carbonitrile can be employed in the synthesis of complex organic molecules through diverse transformation reactions, including halogenation, cross-coupling, and cyclization processes. Its strategic placement of functional groups enables selective modifications, allowing chemists to access a wide range of structural motifs efficiently.