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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)-

Boronic acid, octadecyl-

CCCCCCCCCCCCCCCCCCB(O)O Request for Quotation
Chemical Name: Boronic acid, octadecyl-
CAS Number: 4445-09-4
Product Number: AG003TGE(AGN-PC-0JS9VU)
Synonyms:
MDL No:
Molecular Formula: C18H39BO2
Molecular Weight: 298.31206

Identification/Properties

Properties
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
298.318g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
17
Exact Mass:
298.304g/mol
Monoisotopic Mass:
298.304g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
186
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Octadecylboronic acid is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as a crucial building block in organic chemistry, particularly in the formation of carbon-carbon bonds. Octadecylboronic acid is frequently employed in the formation of complex organic structures through reactions with various electrophiles. Its ability to react with aldehydes and ketones makes it an essential component in the creation of diverse organic molecules. Additionally, Octadecylboronic acid has found applications in Suzuki coupling reactions, where it participates as a key reagent in the production of biaryl compounds. Overall, the use of Octadecylboronic acid in chemical synthesis showcases its significance in enabling the construction of intricate organic frameworks and facilitating the development of novel compounds.