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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-(4-chlorophenoxy)phenyl]-

Clc1ccc(cc1)Oc1ccc(cc1)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-[4-(4-chlorophenoxy)phenyl]-
CAS Number: 41150-48-5
Product Number: AG0073B1(AGN-PC-0KKLZX)
Synonyms:
MDL No:
Molecular Formula: C14H11ClO2
Molecular Weight: 246.6889

Identification/Properties

Computed Properties
Molecular Weight:
246.69g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
246.045g/mol
Monoisotopic Mass:
246.045g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
251
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

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Chemical Structure


The compound 1-(4-(4-Chlorophenoxy)phenyl)ethanone, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound exhibits robust reactivity, making it an ideal intermediate in the synthesis of various organic compounds.One significant application of $name$ in chemical synthesis is its role as a key starting material for the preparation of biologically active molecules. Due to its structural features, $name$ can undergo diverse chemical transformations, such as acylation, reduction, and functional group interconversion, enabling the synthesis of complex molecular structures with high efficiency.Furthermore, $name$ can serve as a valuable precursor for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Its ability to participate in diverse chemical reactions opens up possibilities for creating novel compounds with enhanced functionalities and applications in various industrial sectors.In conclusion, the compound 1-(4-(4-Chlorophenoxy)phenyl)ethanone, or $name$, is a versatile intermediate in chemical synthesis, playing a crucial role in the development of innovative compounds with a wide range of applications.