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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)-

2-(2-fluorophenyl)pyrimidine-5-carbaldehyde

O=Cc1cnc(nc1)c1ccccc1F Request for Quotation
Chemical Name: 2-(2-fluorophenyl)pyrimidine-5-carbaldehyde
CAS Number: 946707-17-1
Product Number: AG006T7L(AGN-PC-01KW4M)
Synonyms:
MDL No:
Molecular Formula: C11H7FN2O
Molecular Weight: 202.1845

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
202.188g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
202.054g/mol
Monoisotopic Mass:
202.054g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
217
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde is a versatile compound widely used in chemical synthesis as a key building block. Its reactive aldehyde group allows for facile functionalization through various reaction pathways, making it a valuable intermediate in the preparation of diverse organic molecules. This compound can participate in condensation reactions to form heterocyclic compounds, such as pyrimidine derivatives, which are important structural motifs in pharmaceuticals and agrochemicals. Additionally, the aromatic fluorophenyl group provides an opportunity for further derivatization, enabling the synthesis of more complex structures with tailored properties. In summary, 2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde serves as a crucial component in the creation of novel compounds through strategic chemical transformations in synthetic organic chemistry.