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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)-

1,4-Pentadien-3-one, 1,5-bis(4-methoxyphenyl)-

COc1ccc(cc1)C=CC(=O)C=Cc1ccc(cc1)OC Request for Quotation
Chemical Name: 1,4-Pentadien-3-one, 1,5-bis(4-methoxyphenyl)-
CAS Number: 2051-07-2
Product Number: AG0029UJ(AGN-PC-0JLCO0)
Synonyms:
MDL No:
Molecular Formula: C19H18O3
Molecular Weight: 294.3444

Identification/Properties

Properties
MP:
136-138°C
Storage:
2-8℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
294.35g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
294.126g/mol
Monoisotopic Mass:
294.126g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
348
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,5-Bis(4-methoxyphenyl)penta-1,4-dien-3-one, also known as $name$, is a versatile compound widely employed in chemical synthesis. Its unique structure and reactivity make it a valuable building block in organic chemistry.In chemical synthesis, 1,5-Bis(4-methoxyphenyl)penta-1,4-dien-3-one serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. It can undergo diverse chemical transformations such as nucleophilic addition, Michael addition, and cross-coupling reactions to yield complex molecular structures with potential biological activities.Furthermore, the electron-rich nature of the methoxyphenyl groups in 1,5-Bis(4-methoxyphenyl)penta-1,4-dien-3-one facilitates its involvement in cascade reactions and heterocycle formation, allowing for the efficient synthesis of heterocyclic compounds and natural product derivatives.Overall, the strategic incorporation of 1,5-Bis(4-methoxyphenyl)penta-1,4-dien-3-one in chemical synthesis enables the rapid construction of diverse molecular scaffolds, making it a valuable tool for synthetic chemists in the development of novel compounds for various applications.