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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)-

Benzene, 1-(2-bromoethyl)-4-chloro-

BrCCc1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzene, 1-(2-bromoethyl)-4-chloro-
CAS Number: 6529-53-9
Product Number: AG003L7O(AGN-PC-0JKGT4)
Synonyms:
MDL No:
Molecular Formula: C8H8BrCl
Molecular Weight: 219.5061

Identification/Properties

Properties
BP:
239.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
219.506g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
217.95g/mol
Monoisotopic Mass:
217.95g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
87.3
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-(2-Bromoethyl)-4-chlorobenzene is a versatile chemical compound often used in organic synthesis as a building block for the creation of various pharmaceuticals, agrochemicals, and advanced materials. This compound serves as an important intermediate in the production of complex organic molecules due to its unique chemical properties and reactivity.One significant application of 1-(2-Bromoethyl)-4-chlorobenzene is in the synthesis of biologically active compounds. By functionalizing the bromoethyl and chlorobenzene moieties, chemists can introduce specific functional groups or structural motifs that are crucial for enhancing the pharmacological or biological properties of the target molecules. This makes 1-(2-Bromoethyl)-4-chlorobenzene a valuable starting material for drug discovery and development efforts.Additionally, this compound is frequently employed in the construction of specialty chemicals and fine chemicals that are used in a wide range of industries. The presence of both a bromoethyl group and a chlorobenzene group in 1-(2-Bromoethyl)-4-chlorobenzene allows for diverse chemical transformations, such as nucleophilic substitution and cross-coupling reactions, enabling the synthesis of a variety of structurally complex and functionally diverse compounds.Furthermore, 1-(2-Bromoethyl)-4-chlorobenzene can be utilized in material science applications for the preparation of advanced materials with tailored properties. Through controlled modifications and polymerization reactions involving this compound, researchers can generate novel polymers, resins, and coatings that exhibit specific mechanical, thermal, or optical characteristics, suitable for various industrial applications.In summary, the use of 1-(2-Bromoethyl)-4-chlorobenzene in chemical synthesis offers a wide range of possibilities for designing and synthesizing diverse compounds with applications in pharmaceuticals, agrochemicals, materials science, and other fields that require the creation of complex organic molecules.