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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-nitrophenyl)-

O=Cc1ccc(o1)c1ccccc1[N+](=O)[O-] Request for Quotation
Chemical Name: 2-Furancarboxaldehyde, 5-(2-nitrophenyl)-
CAS Number: 20000-96-8
Product Number: AG002CHV(AGN-PC-0JUR2M)
Synonyms:
MDL No:
Molecular Formula: C11H7NO4
Molecular Weight: 217.1776

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
217.18g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
217.038g/mol
Monoisotopic Mass:
217.038g/mol
Topological Polar Surface Area:
76A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
276
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 5-(2-Nitrophenyl)furan-2-carbaldehyde compound is widely utilized in chemical synthesis as a versatile building block due to its unique structural properties. It serves as a key intermediate in the production of various organic molecules, particularly in the synthesis of pharmaceuticals, agrochemicals, and functional materials.One of the primary applications of 5-(2-Nitrophenyl)furan-2-carbaldehyde is in the synthesis of heterocyclic compounds. By reacting this compound with different reagents or functional groups, chemists can construct complex heterocycles with diverse properties and functionalities. This versatility makes it a valuable tool in drug discovery and development, as many biologically active molecules contain heterocyclic motifs.Additionally, the presence of the nitrophenyl group in 5-(2-Nitrophenyl)furan-2-carbaldehyde can serve as a directing or activating group in various chemical transformations. This enables selective functionalization at specific positions within the molecule, allowing chemists to tailor the structure of the final product for specific applications.Overall, the strategic incorporation of 5-(2-Nitrophenyl)furan-2-carbaldehyde in chemical synthesis enables the efficient construction of intricate molecular architectures with tailored properties, making it a crucial component in the development of novel compounds across a range of fields.