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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)-

2-Propen-1-one, 3-(4-chlorophenyl)-1-phenyl-

Clc1ccc(cc1)/C=C/C(=O)c1ccccc1 Request for Quotation
Chemical Name: 2-Propen-1-one, 3-(4-chlorophenyl)-1-phenyl-
CAS Number: 956-04-7
Product Number: AG003L75(AGN-PC-0JM18K)
Synonyms:
MDL No:
Molecular Formula: C15H11ClO
Molecular Weight: 242.7002

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
242.702g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
242.05g/mol
Monoisotopic Mass:
242.05g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
271
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(4-Chlorophenyl)-1-phenylprop-2-en-1-one, also known as $name$, is a versatile compound with significant applications in chemical synthesis. This compound is commonly used as a key building block in the pharmaceutical industry for the synthesis of various drug molecules. Its unique structure and reactivity make it a valuable intermediate in the preparation of diverse bioactive compounds.In chemical synthesis, $name$ serves as a crucial starting material for the production of heterocyclic compounds, which are essential in the development of new pharmaceuticals and agrochemicals. Its conjugated system allows for facile functionalization, enabling the introduction of different chemical groups to modulate the properties of the final molecule. Additionally, the presence of the phenyl and chlorophenyl groups provides opportunities for further derivatization, enhancing the versatility of this compound.Moreover, the specific substitution pattern of $name$ offers selective reactivity in various synthetic transformations, allowing chemists to control regioselectivity and stereoselectivity in complex molecule construction. By incorporating 3-(4-Chlorophenyl)-1-phenylprop-2-en-1-one into synthetic routes, researchers can access structurally diverse compounds with potential biological activities.Overall, the application of 3-(4-Chlorophenyl)-1-phenylprop-2-en-1-one in chemical synthesis plays a crucial role in the development of novel compounds with pharmacological relevance and demonstrates its importance as a valuable tool for medicinal chemistry and drug discovery efforts.