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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-methyl-4-nitrophenyl)-

O=Cc1ccc(o1)c1ccc(cc1C)[N+](=O)[O-] Request for Quotation
Chemical Name: 2-Furancarboxaldehyde, 5-(2-methyl-4-nitrophenyl)-
CAS Number: 329222-70-0
Product Number: AG00BZ7Q(AGN-PC-0JTUD5)
Synonyms:
MDL No:
Molecular Formula: C12H9NO4
Molecular Weight: 231.2042

Identification/Properties

Computed Properties
Molecular Weight:
231.207g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
231.053g/mol
Monoisotopic Mass:
231.053g/mol
Topological Polar Surface Area:
76A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
301
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


5-(2-Methyl-4-nitrophenyl)furan-2-carbaldehyde is a versatile compound that finds widespread application in chemical synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. It is particularly valued for its role in the synthesis of heterocyclic compounds, which are essential structural motifs in a wide range of bioactive molecules.In chemical synthesis, 5-(2-Methyl-4-nitrophenyl)furan-2-carbaldehyde can be used as a starting material for the construction of complex molecular architectures. Its unique structure containing a furan ring and a nitrophenyl group provides opportunities for further functionalization and diversification through various chemical transformations. This compound is commonly employed as a precursor for the synthesis of novel compounds with promising biological activities.Furthermore, 5-(2-Methyl-4-nitrophenyl)furan-2-carbaldehyde is utilized in the preparation of fluorescent dyes, ligands for catalysis, and other specialty chemicals. Its strategic placement of functional groups makes it a valuable intermediate in the development of new materials and molecules with specific properties.Overall, the application of 5-(2-Methyl-4-nitrophenyl)furan-2-carbaldehyde in chemical synthesis showcases its importance as a versatile building block for the construction of diverse compounds with applications in the pharmaceutical, agrochemical, and materials science industries.