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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-(5-bromo-2-chlorophenyl)-

Brc1ccc(c(c1)C(=O)C)Cl Request for Quotation
Chemical Name: Ethanone, 1-(5-bromo-2-chlorophenyl)-
CAS Number: 105884-19-3
Product Number: AG008SWF(AGN-PC-00NGJG)
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(5-Bromo-2-chlorophenyl)ethanone, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis. This compound serves as a key building block in organic chemistry and is utilized in various reactions to create complex molecules with specific properties. In chemical synthesis, $name$ is often employed as a precursor in the formation of biologically active compounds, pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it an essential component in the production of a wide range of organic compounds. Additionally, $name$ can be utilized in cross-coupling reactions, substitution reactions, and other transformations to introduce the 5-bromo-2-chlorophenyl group into target molecules, allowing for the synthesis of novel chemical entities. Its role as a synthetic intermediate makes $name$ a valuable tool for chemists in the design and development of new compounds with desirable properties.