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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(2H)-Naphthalenone, 4-(3,4-dichlorophenyl)-3,4-dihydro-

O=C1CCC(c2c1cccc2)c1ccc(c(c1)Cl)Cl Request for Quotation
Chemical Name: 1(2H)-Naphthalenone, 4-(3,4-dichlorophenyl)-3,4-dihydro-
CAS Number: 79560-19-3
Product Number: AG005JBQ(AGN-PC-0BXAYP)
Synonyms:
MDL No:
Molecular Formula: C16H12Cl2O
Molecular Weight: 291.1719

Identification/Properties

Properties
MP:
97-99 °C
BP:
403 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
291.171g/mol
XLogP3:
4.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
290.027g/mol
Monoisotopic Mass:
290.027g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
344
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3,4-Dichlorophenyl)-3,4-dihydronaphthalen-1(2H)-one, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a valuable building block in the synthesis of various pharmacologically active molecules and organic compounds. Its substituted naphthalene ring provides a stable core for the introduction of functional groups and enables the formation of diverse chemical derivatives with specific properties.In chemical synthesis, $name$ is commonly employed as a key intermediate in the preparation of complex organic molecules, such as pharmaceuticals, agrochemicals, and specialty chemicals. The presence of the dichlorophenyl group and the dihydronaphthalenone moiety in this compound offers opportunities for selective chemical transformations, including C-C and C-O bond formation, hydrogenation reactions, and halogenation processes.Furthermore, the unique structural features of $name$ make it a valuable precursor for the synthesis of biologically active compounds with potential therapeutic applications. Its molecular structure can be modified through various chemical reactions to enhance specific properties, such as biological activity, solubility, and stability. As a result, $name$ plays a crucial role in the development of new drug candidates and functional organic materials through rational chemical design and optimization strategies.Overall, the application of 4-(3,4-Dichlorophenyl)-3,4-dihydronaphthalen-1(2H)-one in chemical synthesis offers a wide range of opportunities for the creation of novel organic compounds with diverse functionalities and applications in the fields of medicinal chemistry, materials science, and agrochemical research.