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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)-

1-Butanone, 2-(4-hydroxyphenyl)-1-phenyl-

CCC(C(=O)c1ccccc1)c1ccc(cc1)O Request for Quotation
Chemical Name: 1-Butanone, 2-(4-hydroxyphenyl)-1-phenyl-
CAS Number: 82413-28-3
Product Number: AG0052D5(AGN-PC-00NRV6)
Synonyms:
MDL No:
Molecular Formula: C16H16O2
Molecular Weight: 240.2970

Identification/Properties

Properties
MP:
85-87ºC
Storage:
2-8℃;
Computed Properties
Molecular Weight:
240.302g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
240.115g/mol
Monoisotopic Mass:
240.115g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
260
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-(4-Hydroxyphenyl)-1-phenyl-1-butanone is a versatile compound that finds applications in various chemical synthesis processes. This compound is commonly used as a key intermediate in the production of pharmaceuticals, fragrances, and fine chemicals.In pharmaceutical synthesis, 2-(4-Hydroxyphenyl)-1-phenyl-1-butanone serves as a precursor for the synthesis of various medications due to its structural properties and reactivity. It can be utilized in the creation of biologically active molecules, such as inhibitors, modulators, or prodrugs, which target specific biological pathways or disease mechanisms.In fragrance synthesis, this compound contributes to the development of unique scents and aromas by serving as a building block for the creation of fragrant compounds. Its aromatic properties make it a valuable ingredient in the formulation of perfumes, colognes, and other scented products.Furthermore, in the synthesis of fine chemicals, 2-(4-Hydroxyphenyl)-1-phenyl-1-butanone can be employed to create a variety of specialty chemicals with diverse applications. Its versatility and compatibility with different chemical reactions make it a valuable component in the synthesis of custom-made compounds for various industrial purposes.Overall, the application of 2-(4-Hydroxyphenyl)-1-phenyl-1-butanone in chemical synthesis demonstrates its significance as a building block for the production of a wide range of valuable products across different industries.