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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)-

8-BROMOIMIDAZO[1,2-A]PYRIDINE-2-CARBALDE

O=Cc1cn2c(n1)c(Br)ccc2 Request for Quotation
Chemical Name: 8-BROMOIMIDAZO[1,2-A]PYRIDINE-2-CARBALDE
CAS Number: 1194375-12-6
Product Number: AG000IS3(AGN-PC-0WAJSM)
Synonyms:
MDL No:
Molecular Formula: C8H5BrN2O
Molecular Weight: 225.0421

Identification/Properties

Computed Properties
Molecular Weight:
225.045g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
223.959g/mol
Monoisotopic Mass:
223.959g/mol
Topological Polar Surface Area:
34.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is a versatile chemical compound widely used in chemical synthesis as a key building block. Its application in organic chemistry primarily lies in its ability to serve as a valuable precursor for the synthesis of various biologically active molecules and pharmaceutical intermediates. The aldehyde functional group present in this compound enables it to participate in a range of important reactions, including nucleophilic addition, condensation, and Heck coupling reactions, among others. Additionally, the presence of the imidazo[1,2-a]pyridine scaffold in its structure imparts unique reactivity and functionality, making it highly valuable in the development of novel compounds with diverse biological activities. Through strategic manipulation of its structure, chemists can access a wide array of derivatives with tailored properties, making 8-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde a valuable and versatile tool in the synthesis of complex organic molecules.