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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, [2-(1-methylethyl)phenyl]-

CC(c1ccccc1B(O)O)C Request for Quotation
Chemical Name: Boronic acid, [2-(1-methylethyl)phenyl]-
CAS Number: 89787-12-2
Product Number: AG003ZW5(AGN-PC-07HAGF)
Synonyms:
MDL No: MFCD03411937
Molecular Formula: C9H13BO2
Molecular Weight: 164.0093

Identification/Properties

Properties
MP:
85-86 °C
BP:
297.2 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
164.011g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
164.101g/mol
Monoisotopic Mass:
164.101g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
137
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-Isopropylphenyl)boronic acid, also known as cumylboronic acid, is a versatile compound widely used in chemical synthesis due to its reactivity and unique properties. With its boronic acid functional group, it serves as a valuable building block for preparing a wide range of organic molecules through various synthetic methodologies. One of the key applications of (2-Isopropylphenyl)boronic acid is in Suzuki-Miyaura cross-coupling reactions, a powerful tool in modern organic chemistry for forming carbon-carbon bonds.In Suzuki-Miyaura cross-coupling reactions, (2-Isopropylphenyl)boronic acid acts as a boronate ester partner, undergoing a palladium-catalyzed coupling with various aryl halides or pseudohalides. This versatile transformation allows for the creation of complex organic molecules with high efficiency and selectivity. The ease of functional group tolerance and mild reaction conditions make (2-Isopropylphenyl)boronic acid an excellent choice for constructing biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, materials science, and other fields of chemistry.Furthermore, (2-Isopropylphenyl)boronic acid can also participate in other types of reactions such as borylation, arylation, and cyclization reactions, further expanding its utility in organic synthesis. Its ability to introduce the isopropyl group and boron atom into the target molecules imparts unique properties and functionalities, making it an indispensable tool for designing and synthesizing novel compounds for various applications in the chemical industry.