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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, (2,5-dichlorophenyl)phenyl-

Clc1ccc(c(c1)C(=O)c1ccccc1)Cl Request for Quotation
Chemical Name: Methanone, (2,5-dichlorophenyl)phenyl-
CAS Number: 16611-67-9
Product Number: AG001WI5(AGN-PC-0JRGHK)
Synonyms:
MDL No: MFCD00079746
Molecular Formula: C13H8Cl2O
Molecular Weight: 251.1080

Identification/Properties

Properties
MP:
87-88 °C
BP:
369.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2,5-Dichlorophenyl)(phenyl)methanone, also known as $name$, is a versatile reagent commonly utilized in chemical synthesis. Its unique molecular structure allows for a variety of reactions and transformations in organic chemistry.$name$ is frequently employed as a key intermediate in the synthesis of complex organic molecules due to its ability to undergo different chemical reactions leading to diverse functional groups. Its presence in a reaction mixture can facilitate the formation of new carbon-carbon and carbon-heteroatom bonds, making it invaluable in the construction of intricate molecular architectures.In addition, $name$ can act as a valuable building block for the creation of pharmaceuticals, agrochemicals, and materials. Its use in the production of specialty chemicals highlights its significance in the development of innovative products with diverse applications.Furthermore, the reactivity and stability of $name$ make it a preferred choice for chemists seeking reliable and efficient methods for introducing functional groups into organic molecules. Its compatibility with a range of reaction conditions and substrates make it a versatile tool for synthetic chemists looking to streamline their processes and enhance synthetic efficiency.Overall, the application of (2,5-Dichlorophenyl)(phenyl)methanone in chemical synthesis underscores its importance as a fundamental building block in organic chemistry, enabling the creation of complex molecules with precision and control.