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  2. 2H-Pyran-2,6(3H)-dione, 4-(4-chlorophenyl)dihydro-

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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)-

2H-Pyran-2,6(3H)-dione, 4-(4-chlorophenyl)dihydro-

O=C1CC(CC(=O)O1)c1ccc(cc1)Cl Request for Quotation
Chemical Name: 2H-Pyran-2,6(3H)-dione, 4-(4-chlorophenyl)dihydro-
CAS Number: 53911-68-5
Product Number: AG00D83J(AGN-PC-07Y4FW)
Synonyms:
MDL No:
Molecular Formula: C11H9ClO3
Molecular Weight: 224.6404

Identification/Properties

Properties
MP:
128-130°C
BP:
393.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
224.64g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
224.024g/mol
Monoisotopic Mass:
224.024g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
253
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


In chemical synthesis, 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione, also known as $name$, serves as a valuable building block for creating complex organic compounds. Its unique structure and reactivity make it an essential component in the formation of diverse molecules with specific functional groups and properties. By incorporating $name$ into various synthetic pathways, chemists can access a wide array of potential derivatives that exhibit promising biological activities or material properties. Its inclusion in multistep synthesis processes enables the efficient construction of intricate molecular architectures for applications in drug discovery, materials science, and biochemical research.