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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)-

Methanone, (3-nitrophenyl)phenyl-

O=C(c1cccc(c1)[N+](=O)[O-])c1ccccc1 Request for Quotation
Chemical Name: Methanone, (3-nitrophenyl)phenyl-
CAS Number: 2243-80-3
Product Number: AG003JT7(AGN-PC-00FBLM)
Synonyms:
MDL No:
Molecular Formula: C13H9NO3
Molecular Weight: 227.2155

Identification/Properties

Properties
MP:
92-94℃
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
227.219g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
227.058g/mol
Monoisotopic Mass:
227.058g/mol
Topological Polar Surface Area:
62.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
292
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


(3-Nitrophenyl)(phenyl)methanone, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound is predominantly employed as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Due to its unique chemical structure, $name$ serves as a crucial intermediate in the synthesis of complex organic molecules.In organic synthesis, $name$ is utilized as a starting material to introduce the nitrophenyl and phenyl groups into the desired molecular architecture. Its reactivity and compatibility with a wide range of functional groups make it an essential component in the development of novel chemical compounds with diverse applications. By incorporating $name$ into synthetic pathways, chemists can tailor the properties and functions of the final products to meet specific requirements.Furthermore, the presence of the nitro group in $name$ allows for further functionalization through various chemical transformations, enabling the synthesis of structurally intricate molecules. This versatility makes $name$ a valuable tool for the efficient construction of complex organic frameworks in a controlled and precise manner. Its role in chemical synthesis extends across multiple industries, including pharmaceuticals, materials science, and agrochemicals, highlighting its significance in modern chemistry.