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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)-

Ethanone,1-(3-bromo-5-chlorophenyl)-

Clc1cc(Br)cc(c1)C(=O)C Request for Quotation
Chemical Name: Ethanone,1-(3-bromo-5-chlorophenyl)-
CAS Number: 154257-85-9
Product Number: AG007GB8(AGN-PC-0Q6OKE)
Synonyms:
MDL No:
Molecular Formula: C8H6BrClO
Molecular Weight: 233.4896

Identification/Properties

Computed Properties
Molecular Weight:
233.489g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
231.929g/mol
Monoisotopic Mass:
231.929g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
160
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


1-(3-Bromo-5-chlorophenyl)ethanone, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the production of complex organic compounds. In chemical synthesis, 1-(3-Bromo-5-chlorophenyl)ethanone can be utilized as a key starting material in the formation of diverse molecular structures, allowing for the efficient and controlled synthesis of target molecules. Its ability to undergo various chemical reactions, such as substitution, addition, and condensation reactions, enables chemists to manipulate its structure and design new compounds with specific properties. Overall, the application of 1-(3-Bromo-5-chlorophenyl)ethanone in chemical synthesis plays a significant role in the creation of advanced materials and compounds for industrial and research purposes.