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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-cyclohexylethenylboronic acid

OB(C(=C)C1CCCCC1)O Request for Quotation
Chemical Name: 1-cyclohexylethenylboronic acid
CAS Number: 1202245-69-9
Product Number: AG009425(AGN-PC-0AC0ZF)
Synonyms:
MDL No:
Molecular Formula: C8H15BO2
Molecular Weight: 154.0145

Identification/Properties

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-Cyclohexylvinyl)boronic acid, also known as cyclohexenylboronic acid, is a versatile reagent widely used in organic synthesis for the formation of carbon-carbon bonds through versatile cross-coupling reactions. This compound serves as a valuable building block in the construction of complex organic molecules due to its ability to undergo efficient Suzuki-Miyaura reactions with various electrophiles such as aryl halides and vinyl halides. Additionally, (1-Cyclohexylvinyl)boronic acid can be utilized in Heck reactions, Sonogashira reactions, and other palladium-catalyzed coupling reactions to introduce the cyclohexenyl moiety into organic frameworks. Its compatibility with various functional groups and mild reaction conditions make it a valuable tool in the assembly of pharmaceuticals, agrochemicals, and advanced materials.