Boronic acid derivatives
![Frontier Specialty Chemicals 1g, 2-Methylprop-1-enylboronic acid pinacol ester, 98%, [126689-00-7], M11191 182.068 C10H19BO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 1g, 2-Methylprop-1-enylboronic acid pinacol ester, 98%, [126689-00-7], M11191 182.068 C10H19BO2
Compound: 2-Methylprop-1-enylboronic acid pinacol ester
CAS#: 126689-00-7
MDL#: not listed
Background: A branched alkenylboronic ester used as a Suzuki-Miyaura coupling partner in organic synthesis. It provides a convenient means to introduce an isobutenyl group into pharmaceutical and materials science building blocks.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 5g, 1-Pentenylboronic acid, 98%, [104376-24-1], P11073 113.951 C5H11BO2
Compound: 1-Pentenylboronic acid
CAS#: 104376-24-1
MDL#: not listed
Background: A terminal alkenylboronic acid used as a Suzuki-Miyaura coupling partner in organic synthesis. It provides a convenient means to introduce a pentenyl group into pharmaceutical and agrochemical building blocks.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, n-Propylboronic acid, 98%, [17745-45-8], P6700 87.91 C3H9BO2
Compound: n-Propylboronic acid
CAS#: 17745-45-8
MDL#: MFCD01074564
Background: n-Propylboronic acid is an alkylboronic acid used as a reagent in Suzuki cross-coupling reactions to form carbon-carbon bonds in pharmaceutical and agrochemical synthesis. It has been used to prepare mTOR inhibitors for anti-tumor research and endothelial lipase inhibitors. It has also been studied for its ability to inhibit serine proteases such as thrombin.
Frontier Specialty Chemicals 5g, 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester, 98%, [847818-74-0], M2011 208.07 C10H17BN2O2
Compound: 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
CAS#: 847818-74-0
MDL#: MFCD05861380
Background: A methylated pyrazole boronic ester used as a coupling partner in Suzuki-Miyaura reactions. It has been used in the stereoselective preparation of arylamide compounds studied as cathepsin inhibitors, supporting medicinal chemistry research.
Storage: Store at 2-8°C, under dry conditions.
Aobchem 4-Methoxy-2-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1073353-81-7 | C13H18BNO5 | 250mg
4-Methoxy-2-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1073353-81-7 | C13H18BNO5 | 250mg
Frontier Specialty Chemicals 25g, 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester, 98%, [847818-74-0], M2011 208.07 C10H17BN2O2
Compound: 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
CAS#: 847818-74-0
MDL#: not listed
Background: An N-methylated pyrazole boronic ester used as a Suzuki-Miyaura coupling partner in pharmaceutical research. It provides direct access to substituted pyrazole-containing scaffolds in drug discovery synthesis.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 5g, 3-Chloropyridine-4-boronic acid hydrate, 96%, [1256355-22-2], C1827 175.378 C5H7BClNO3
Compound: 3-Chloropyridine-4-boronic acid hydrate
CAS#: 1256355-22-2
MDL#: MFCD03453058
Background: 3-Chloropyridine-4-boronic acid hydrate is offered for experimental and research use as a synthetic building block in organic chemistry. Like related chloropyridine boronic acid derivatives, it is used in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceutical and agrochemical development.
Frontier Specialty Chemicals 5g, Cyclohexylboronic acid, 99%, [4441-56-9], C4722 127.98 C6H13BO2
Compound: Cyclohexylboronic acid
CAS#: 4441-56-9
MDL#: MFCD01311824
Background: Cyclohexylboronic acid is an alkylboronic acid used as a reagent in Suzuki cross-coupling reactions to form carbon-carbon bonds. It supports the synthesis of biaryl and alkyl-aryl compounds relevant to pharmaceuticals, agrochemicals, and materials science. It is also used in the arylation and alkylation of heterocyclic scaffolds such as diphenylisoxazole.
Frontier Specialty Chemicals 1g, Cyclohexylboronic acid, 99%, [4441-56-9], C4722 127.98 C6H13BO2
Compound: Cyclohexylboronic acid
CAS#: 4441-56-9
MDL#: MFCD01311824
Background: Cyclohexylboronic acid is an alkylboronic acid used as a reagent in Suzuki cross-coupling reactions to form carbon-carbon bonds. It supports the synthesis of biaryl and alkyl-aryl compounds relevant to pharmaceuticals, agrochemicals, and materials science. It is also used in the arylation and alkylation of heterocyclic scaffolds such as diphenylisoxazole.
Frontier Specialty Chemicals 25g, Cyclohexylboronic acid pinacol ester, >95%, [87100-15-0], C1155 210.12 C12H23BO2
Compound: Cyclohexylboronic acid pinacol ester
CAS#: 87100-15-0
MDL#: MFCD04038749
Background: Cyclohexylboronic acid pinacol ester is used as a ligand and coupling partner in Suzuki cross-coupling reactions in organic synthesis. Its pinacol ester form provides improved stability and handling compared to the free boronic acid, making it a useful research chemical for proteomics and synthetic chemistry applications.
Frontier Specialty Chemicals 1g, 3,3-Diethoxy-1-propenylboronic acid pinacol ester, 95%, [153737-25-8], D10252 256.146 C13H25BO4
Compound: 3,3-Diethoxy-1-propenylboronic acid pinacol ester
CAS#: 153737-25-8
MDL#: MFCD03788737
Background: An acetal-protected propenylboronic ester used as a synthetic and pharmaceutical intermediate. It participates in Suzuki-Miyaura cross-coupling reactions, and the diethyl acetal group can be hydrolyzed after coupling to reveal an aldehyde for further derivatization.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 25g, 3-Chloropyridine-4-boronic acid hydrate, 96%, [1256355-22-2], C1827 175.378 C5H7BClNO3
Compound: 3-Chloropyridine-4-boronic acid hydrate
CAS#: 1256355-22-2
MDL#: MFCD03453058
Background: 3-Chloropyridine-4-boronic acid hydrate is offered for experimental and research use as a synthetic building block in organic chemistry. Like related chloropyridine boronic acid derivatives, it is used in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceutical and agrochemical development.
Frontier Specialty Chemicals 5g, Naphthalene-2-boronic acid, 98%, [32316-92-0], N6183 171.99 C10H9BO2
Compound: Naphthalene-2-boronic acid
CAS#: 32316-92-0
MDL#: MFCD00236051
Background: Naphthalene-2-boronic acid is a synthetic fine chemical used in the synthesis of pharmaceuticals and fine organic chemicals. It serves as a coupling partner in Suzuki-Miyaura and other organoboron cross-coupling reactions to form carbon-carbon bonds. It has also been used in the development of N-heterocyclic carbene ligands and organic light-emitting diode materials.
Storage: Store at 2-8°C under dry conditions.
Frontier Specialty Chemicals 5g, n-Propylboronic acid, 98%, [17745-45-8], P6700 87.91 C3H9BO2
Compound: n-Propylboronic acid
CAS#: 17745-45-8
MDL#: MFCD01074564
Background: n-Propylboronic acid is an alkylboronic acid used as a reagent in Suzuki cross-coupling reactions to form carbon-carbon bonds in pharmaceutical and agrochemical synthesis. It has been used to prepare mTOR inhibitors for anti-tumor research and endothelial lipase inhibitors. It has also been studied for its ability to inhibit serine proteases such as thrombin.
Frontier Specialty Chemicals 1g, Dibenzofuran-4-boronic acid, 97%, [100124-06-9], D5438 212.01 C12H9BO3
Compound: Dibenzofuran-4-boronic acid
CAS#: 100124-06-9
MDL#: MFCD00092336
Background: Dibenzofuran-4-boronic acid is a heteroaryl boronic acid used as a coupling partner in Suzuki-Miyaura cross-coupling reactions to form biaryl and heterobiaryl structures. It has been used to prepare glycosensors, as its fluorescence changes upon binding sugars under near-physiological conditions. It also serves as an intermediate in pharmaceutical, agrochemical, and OLED material synthesis.