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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)-

BENZYL 4-CHLOROPHENYL KETONE

Clc1ccc(cc1)C(=O)Cc1ccccc1 Request for Quotation
Chemical Name: BENZYL 4-CHLOROPHENYL KETONE
CAS Number: 1889-71-0
Product Number: AG002HHK(AGN-PC-0WAKG8)
Synonyms:
MDL No:
Molecular Formula: C14H11ClO
Molecular Weight: 230.6895

Identification/Properties

Properties
MP:
103-107 °C(lit.)
BP:
365.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
230.691g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
230.05g/mol
Monoisotopic Mass:
230.05g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
225
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


Benzyl 4-chlorophenyl ketone, commonly known as a benzophenone derivative, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, this compound serves as a key intermediate in the formation of various organic molecules. In chemical synthesis, Benzyl 4-chlorophenyl ketone is frequently utilized as a precursor in the production of pharmaceuticals, agrochemicals, fragrances, and advanced materials. Its reactivity allows for selective functional group transformations, making it a valuable tool in the synthesis of complex organic compounds. Furthermore, Benzyl 4-chlorophenyl ketone can be employed as a starting material for the construction of heterocyclic compounds and other structurally diverse molecules in the realm of organic synthesis. Its ability to participate in various synthetic pathways makes it an essential component in the toolkit of organic chemists striving to create innovative and diverse chemical entities for a wide range of applications.