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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)-

1-(1-BROMOETHYL)-4-CHLOROBENZENE

CC(c1ccc(cc1)Cl)Br Request for Quotation
Chemical Name: 1-(1-BROMOETHYL)-4-CHLOROBENZENE
CAS Number: 14804-61-6
Product Number: AG001FE6(AGN-PC-0WAM0Y)
Synonyms:
MDL No:
Molecular Formula: C8H8BrCl
Molecular Weight: 219.5061

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
219.506g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
217.95g/mol
Monoisotopic Mass:
217.95g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.4
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(1-Bromoethyl)-4-chlorobenzene is a versatile chemical compound widely used in chemical synthesis processes. Its primary application lies in the field of organic chemistry, where it serves as a valuable building block for the creation of various complex molecules. This compound plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and materials science.Due to its unique structural features, 1-(1-Bromoethyl)-4-chlorobenzene can participate in a wide range of chemical reactions, such as nucleophilic substitution, Suzuki coupling, and Heck reactions. These reactions enable the attachment of different functional groups to the benzene ring, allowing for the creation of diverse organic compounds with specific properties and applications.Furthermore, 1-(1-Bromoethyl)-4-chlorobenzene is a key intermediate in the production of various fine chemicals and specialty materials. Its ability to undergo selective transformations under controlled conditions makes it a valuable tool for chemists and researchers exploring new avenues in synthetic chemistry.Overall, the application of 1-(1-Bromoethyl)-4-chlorobenzene in chemical synthesis represents a fundamental aspect of modern organic chemistry, enabling the development of novel compounds with potential applications in various industries.