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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-bromoethenyl)-4-chloro-

BrC=Cc1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzene, 1-(2-bromoethenyl)-4-chloro-
CAS Number: 125428-11-7
Product Number: AG000NPD(AGN-PC-00B3HE)
Synonyms:
MDL No:
Molecular Formula: C8H6BrCl
Molecular Weight: 217.4902

Identification/Properties

Computed Properties
Molecular Weight:
217.49g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
215.934g/mol
Monoisotopic Mass:
215.934g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1
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-(2-Bromoethenyl)-4-chlorobenzene, also known as $name$, is a versatile chemical compound widely used in organic synthesis. Its unique structure and reactivity make it a valuable building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. In chemical synthesis, $name$ serves as a key intermediate in the preparation of diverse organic compounds. Its ability to undergo various reactions, such as substitutions, additions, and coupling reactions, allows for the efficient and selective formation of complex molecular structures. By incorporating $name$ into synthetic routes, chemists can access a wide range of functionalized molecules with diverse applications in the fields of medicine, materials science, and beyond.