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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)-

4-(5-bromopyrimidin-2-yl)oxybenzaldehyde

O=Cc1ccc(cc1)Oc1ncc(cn1)Br Request for Quotation
Chemical Name: 4-(5-bromopyrimidin-2-yl)oxybenzaldehyde
CAS Number: 952182-73-9
Product Number: AG00IIUF(AGN-PC-04HB5E)
Synonyms:
MDL No:
Molecular Formula: C11H7BrN2O2
Molecular Weight: 279.0895

Identification/Properties

Computed Properties
Molecular Weight:
279.093g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
277.969g/mol
Monoisotopic Mass:
277.969g/mol
Topological Polar Surface Area:
52.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
224
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


4-((5-Bromopyrimidin-2-yl)oxy)benzaldehyde is a versatile compound that finds wide application in chemical synthesis. This aldehyde derivative serves as a valuable building block in the creation of various organic compounds due to its unique structural properties.In organic synthesis, 4-((5-Bromopyrimidin-2-yl)oxy)benzaldehyde can act as a key intermediate for the preparation of heterocyclic compounds. Its functional groups enable it to participate in a range of reactions, including nucleophilic addition, acylation, and condensation reactions, leading to the formation of complex molecular structures.Furthermore, the presence of the bromopyrimidine moiety in the molecule enhances its reactivity and enables selective functionalization at specific positions, offering chemists precise control over the synthetic pathways. This aldehyde can also serve as a fluorescent probe or a ligand in coordination chemistry studies, showcasing its versatility in different fields of chemical research.Overall, 4-((5-Bromopyrimidin-2-yl)oxy)benzaldehyde plays a crucial role in advancing synthetic methodologies and exploring new chemical entities, making it a valuable asset in the toolkit of synthetic chemists and researchers.