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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-(4-bromo-2-chlorophenyl)-

Brc1ccc(c(c1)Cl)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(4-bromo-2-chlorophenyl)-
CAS Number: 252561-81-2
Product Number: AG003650(AGN-PC-00POAO)
Synonyms:
MDL No:
Molecular Formula: C8H6BrClO
Molecular Weight: 233.4896

Identification/Properties

Properties
BP:
265.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
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


2'-Chloro-4'-bromoacetophenone, also known as $name$, is a valuable chemical intermediate commonly utilized in numerous chemical synthesis processes. This compound plays a vital role in the production of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique chemical properties. In organic synthesis, 2'-Chloro-4'-bromoacetophenone is often used as a key building block in the construction of more complex molecules. Its functional groups allow for versatile reactivity, enabling the creation of diverse chemical structures. Additionally, the presence of both chlorine and bromine atoms makes $name$ a versatile substrate for further derivatization through various chemical reactions, such as nucleophilic substitution and cross-coupling reactions. These characteristics make 2'-Chloro-4'-bromoacetophenone an indispensable tool for chemists and researchers seeking to design and develop novel compounds for a wide range of applications.