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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-Bromo-5-chloroethylbenzene

CCc1cc(Cl)ccc1Br Request for Quotation
Chemical Name: 2-Bromo-5-chloroethylbenzene
CAS Number: 1160573-89-6
Product Number: AG01BYV4(AGN-PC-0WGGOH)
Synonyms:
MDL No:
Molecular Formula: C8H8BrCl
Molecular Weight: 219.5061

Identification/Properties

Computed Properties
Molecular Weight:
219.5g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
217.94979g/mol
Monoisotopic Mass:
217.94979g/mol
Topological Polar Surface Area:
0Ų
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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-Bromo-4-chloro-2-ethylbenzene is a versatile compound that finds wide application in chemical synthesis. This compound serves as an important building block in the creation of various organic molecules, particularly in the field of medicinal chemistry. Due to its unique structure and reactivity, 1-Bromo-4-chloro-2-ethylbenzene is utilized in the synthesis of pharmaceutical intermediates, agrochemicals, and other specialty chemicals. It acts as a key precursor in the preparation of complex organic compounds by undergoing different types of chemical reactions such as substitution, elimination, and coupling reactions.In addition, this compound plays a crucial role in the development of new materials and polymers. Its strategic placement of functional groups allows for selective modification and derivatization, enabling the synthesis of tailored molecules with specific properties and functions. Researchers and chemists rely on 1-Bromo-4-chloro-2-ethylbenzene for the construction of diverse molecular architectures with desired characteristics.Overall, the use of 1-Bromo-4-chloro-2-ethylbenzene in chemical synthesis contributes significantly to the advancement of various industries, including pharmaceuticals, agrochemicals, materials science, and more. Its versatility and compatibility with different synthetic methodologies make it a valuable tool for creating innovative molecules and compounds.