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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-Furancarboxaldehyde, 5-(2,5-dichlorophenyl)-

O=Cc1ccc(o1)c1cc(Cl)ccc1Cl Request for Quotation
Chemical Name: 2-Furancarboxaldehyde, 5-(2,5-dichlorophenyl)-
CAS Number: 99113-89-0
Product Number: AG003M3D(AGN-PC-0JUR37)
Synonyms:
MDL No:
Molecular Formula: C11H6Cl2O2
Molecular Weight: 241.0701

Identification/Properties

Computed Properties
Molecular Weight:
241.067g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
239.974g/mol
Monoisotopic Mass:
239.974g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
235
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(2,5-Dichlorophenyl)-2-furaldehyde is a versatile compound commonly used in chemical synthesis as a key building block for various organic reactions. Its unique structure, containing both a furan ring and a dichlorophenyl group, lends itself to a range of applications in the synthesis of pharmaceuticals, agrochemicals, and functional materials.In organic synthesis, 5-(2,5-Dichlorophenyl)-2-furaldehyde serves as a valuable intermediate for the construction of complex molecules due to its reactivity and potential for functional group manipulation. It can be utilized in the preparation of heterocyclic compounds, such as benzofurans and indoles, through cyclization reactions. Additionally, its aldehyde functionality can participate in various transformations, including aldol condensations, Grignard reactions, and Wittig reactions, enabling the creation of diverse chemical structures.Furthermore, the presence of the dichlorophenyl group in 5-(2,5-Dichlorophenyl)-2-furaldehyde offers opportunities for further derivatization, allowing for the introduction of additional substituents that can modulate the compound's properties. This flexibility makes it a valuable tool for medicinal chemists in the design and synthesis of novel pharmaceutical agents with desired pharmacological activities.Overall, 5-(2,5-Dichlorophenyl)-2-furaldehyde plays a crucial role in organic synthesis by enabling the construction of complex molecules with diverse applications in the fields of pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable asset for chemists seeking to access a wide range of chemical structures for various purposes.