Boronic acid derivatives
![Frontier Specialty Chemicals 25g, Ethylboronic acid, 97%, [4433-63-0], E1104 73.89 C2H7BO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 25g, Ethylboronic acid, 97%, [4433-63-0], E1104 73.89 C2H7BO2
Compound: Ethylboronic acid
CAS#: 4433-63-0
MDL#: MFCD01074536
Background: Ethylboronic acid is used as an intermediate in the synthesis of bioactive molecules with anticancer, antiviral, and antibacterial properties, and its derivatives have been studied as inhibitors of bacterial beta-lactamases involved in antibiotic resistance. It is widely used as a reagent in Suzuki-Miyaura cross-coupling reactions, forming carbon-carbon bonds with aryl and vinyl halides under mild conditions, and is also used in analytical chemistry techniques such as chromatography and mass spectrometry.
Frontier Specialty Chemicals 5g, 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.
Frontier Specialty Chemicals 1g, Quinoline-3-boronic acid, 95%, [191162-39-7], Q5061 172.98 C9H8BNO2
Compound: Quinoline-3-boronic acid
CAS#: 191162-39-7
MDL#: MFCD02183527
Background: Quinoline-3-boronic acid is a heteroaryl boronic acid used in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It has served as a reactant in the preparation of HIV protease inhibitors and has shown activity as an inhibitor of the Staphylococcus aureus NorA efflux pump. It is also used as a fluorescent sugar-sensing probe and as an intermediate in OLED materials.
Frontier Specialty Chemicals 1g, Quinoline-5-boronic acid, 98%, [355386-94-6], Q1089 172.98 C9H8BNO2
Compound: Quinoline-5-boronic acid
CAS#: 355386-94-6
MDL#: MFCD03095058
Background: Quinoline-5-boronic acid is used in the fabrication of organic semiconductors, where 5-substituted quinoline derivatives prepared via Suzuki coupling serve as electron-transport and hole-blocking materials in multilayer OLED architectures. It is also applied in the design of chemical sensors, in Suzuki-Miyaura coupling for drug discovery, and as a nitrogen donor ligand in metal-organic framework and fluorescent pH probe construction.
Frontier Specialty Chemicals 25g, 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, Quinoline-3-boronic acid, 95%, [191162-39-7], Q5061 172.98 C9H8BNO2
Compound: Quinoline-3-boronic acid
CAS#: 191162-39-7
MDL#: MFCD02183527
Background: Quinoline-3-boronic acid is a heteroaryl boronic acid used in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It has served as a reactant in the preparation of HIV protease inhibitors and has shown activity as an inhibitor of the Staphylococcus aureus NorA efflux pump. It is also used as a fluorescent sugar-sensing probe and as an intermediate in OLED materials.
Frontier Specialty Chemicals 25g, Methylboronic acid, 98%, [13061-96-6], M7469 59.86 CH5BO2
Compound: Methylboronic acid
CAS#: 13061-96-6
MDL#: MFCD00002105
Background: Methylboronic acid is a simple alkylboronic acid used in Suzuki and Stille cross-coupling reactions to form carbon-carbon bonds in palladium-catalyzed synthesis. It is used in the development of boron-containing pharmaceuticals and agrochemicals, including chrysin analogs and casein kinase I inhibitors. It also serves as a reagent for derivatizing carbohydrates and other biologically active compounds.
Frontier Specialty Chemicals 1g, 3-Cyano-4-fluorophenylboronic acid, 97%, [214210-21-6], C10879 164.93 C7H5BFNO2
Compound: 3-Cyano-4-fluorophenylboronic acid
CAS#: 214210-21-6
MDL#: not listed
Background: A cyano- and fluoro-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. The nitrile group offers a reactive handle for further derivatization of downstream products.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 5g, 3-Cyano-4-fluorophenylboronic acid, 97%, [214210-21-6], C10879 164.93 C7H5BFNO2
Compound: 3-Cyano-4-fluorophenylboronic acid
CAS#: 214210-21-6
MDL#: not listed
Background: A cyano- and fluoro-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. The nitrile group offers a reactive handle for further derivatization of downstream products.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, 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, Cyclopentylboronic acid, 96%, [63076-51-7], C8488 113.95 C5H11BO2
Compound: Cyclopentylboronic acid
CAS#: 63076-51-7
MDL#: MFCD01074541
Background: Cyclopentylboronic acid is a cycloalkylboronic acid used in palladium- and nickel-catalyzed cross-coupling reactions to construct functionalized aromatic and aliphatic hydrocarbons. It participates in reactions with aryl halides, tosylates, and mesylates, including Suzuki-type couplings used in pharmaceutical and fine chemical synthesis. It has also been applied in the arylation and alkylation of heterocyclic scaffolds such as diphenylisoxazole.
Frontier Specialty Chemicals 1g, Cyclopentylboronic acid, 96%, [63076-51-7], C8488 113.95 C5H11BO2
Compound: Cyclopentylboronic acid
CAS#: 63076-51-7
MDL#: MFCD01074541
Background: Cyclopentylboronic acid is a cycloalkylboronic acid used in palladium- and nickel-catalyzed cross-coupling reactions to construct functionalized aromatic and aliphatic hydrocarbons. It participates in reactions with aryl halides, tosylates, and mesylates, including Suzuki-type couplings used in pharmaceutical and fine chemical synthesis. It has also been applied in the arylation and alkylation of heterocyclic scaffolds such as diphenylisoxazole.
Frontier Specialty Chemicals 5g, 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.
Matrix Scientific 4-BOC-AMINOPHENYLBORONIC AC-1G
4-Boc-Aminophenylboronic acid, 1g,C11H16BNO4, MFCD02093054, mw 237.07, [380430-49-9]
Frontier Specialty Chemicals 25g, Dibenzofuran-4-boronic acid, 97%, [100124-06-9], D5438 212.01 C12H9BO3
Compound: Dibenzofuran-4-boronic acid
CAS#: 100124-06-9
MDL#: not listed
Background: A dibenzofuran-substituted boronic acid used as a Suzuki-Miyaura coupling partner in materials science and pharmaceutical research. Dibenzofuran-containing building blocks are commonly used in the synthesis of organic electronic and photoluminescent materials.
Storage: Store at room temperature, under dry conditions.