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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-bromoquinolin-3-yl)boronic acid

OB(c1cc2ccccc2nc1Br)O Request for Quotation
Chemical Name: (2-bromoquinolin-3-yl)boronic acid
CAS Number: 745784-05-8
Product Number: AG003GT0(AGN-PC-01LRIH)
Synonyms:
MDL No:
Molecular Formula: C9H7BBrNO2
Molecular Weight: 251.8724

Identification/Properties

Properties
MP:
144-147 °C
Storage:
Keep in dry area;2-8℃;

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


2-Bromoquinoline-3-boronic acid is a versatile chemical compound that finds widespread application in organic synthesis. As a boronic acid derivative, it serves as a valuable building block in the construction of various biologically active molecules and functional materials. In chemical synthesis, 2-Bromoquinoline-3-boronic acid acts as a key reagent for the formation of carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions. This compound's ability to undergo these coupling reactions makes it a valuable tool for the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and reactivity make it an essential component in the toolkit of synthetic chemists working to develop new molecules with diverse applications.