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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)-

Ethanone, 1-(4-methylphenyl)-2-phenyl-

Cc1ccc(cc1)C(=O)Cc1ccccc1 Request for Quotation
Chemical Name: Ethanone, 1-(4-methylphenyl)-2-phenyl-
CAS Number: 2001-28-7
Product Number: AG002CJK(AGN-PC-0JO764)
Synonyms:
MDL No:
Molecular Formula: C15H14O
Molecular Weight: 210.2711

Identification/Properties

Properties
MP:
108-110°C
BP:
343°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
210.276g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
210.104g/mol
Monoisotopic Mass:
210.104g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
220
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


2-Phenyl-1-(p-tolyl)ethanone, also known as α-methylbenzyl phenyl ketone, is a versatile compound widely utilized in chemical synthesis for various applications. One key use of this compound is as a building block in the synthesis of pharmaceuticals and agrochemicals. It serves as a valuable intermediate in the production of diverse organic compounds due to its structural properties and reactivity. Additionally, 2-Phenyl-1-(p-tolyl)ethanone is employed in the preparation of fragrances and flavors, where its aromatic nature enhances the olfactory profile of final products. Furthermore, this compound can be utilized as a starting material for the development of novel materials with specialized properties, such as liquid crystals or polymers. Its role in chemical synthesis extends to the creation of fine chemicals and specialty products, showcasing its significance in enabling the advancement of various industries.