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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)-

3-Bromo-5-chloro-tert-butylbenzene

Clc1cc(Br)cc(c1)C(C)(C)C Request for Quotation
Chemical Name: 3-Bromo-5-chloro-tert-butylbenzene
CAS Number: 1263377-20-3
Product Number: AG01FE4B(AGN-PC-3H6DGP)
Synonyms:
MDL No:
Molecular Formula: C10H12BrCl
Molecular Weight: 247.5593

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Chemical Structure


1-Bromo-3-(tert-butyl)-5-chlorobenzene serves as a valuable building block in chemical synthesis, specifically in organic chemistry reactions. This compound is commonly utilized as a versatile intermediate in the preparation of various organic molecules due to its unique structural properties. Its strategic placement of bromine, tert-butyl, and chlorine functional groups enables it to participate in a wide range of synthetic transformations, making it a versatile tool for chemists. Amidst the myriad of reactions it can undergo, 1-Bromo-3-(tert-butyl)-5-chlorobenzene is frequently employed in Suzuki coupling reactions, Grignard reactions, and nucleophilic aromatic substitutions. These reactions enable the modification and functionalization of the compound, allowing for the synthesis of complex organic compounds with tailored properties. Through precise manipulation of these reactions, chemists can harness the reactivity and selectivity of 1-Bromo-3-(tert-butyl)-5-chlorobenzene to efficiently construct elaborate molecular architectures and achieve specific chemical goals.