Boronic acid derivatives
![Frontier Specialty Chemicals 1g, 3,5-Dichlorophenylboronic acid, 97%, [67492-50-6], D9266 190.82 C6H5BCl2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 1g, 3,5-Dichlorophenylboronic acid, 97%, [67492-50-6], D9266 190.82 C6H5BCl2O2
Compound: 3,5-Dichlorophenylboronic acid
CAS#: 67492-50-6
MDL#: MFCD00051935
Background: 3,5-Dichlorophenylboronic acid is used as an intermediate in pharmaceutical manufacturing and plays a role in Suzuki-Miyaura cross-coupling reactions essential for developing active pharmaceutical ingredients. It is also a reactant in trifluoromethylation, intramolecular aromatic carbenoid insertion, and cyanation reactions for synthesizing aromatic nitriles. It has additionally been used to facilitate transport of ribonucleosides across liposome membranes in biophysical research.
Frontier Specialty Chemicals 25g, 3-Aminophenylboronic acid monohydrate, 98%, [206658-89-1], A6087 154.96 C6H8BNO2.H2O
Compound: 3-Aminophenylboronic acid monohydrate
CAS#: 206658-89-1
MDL#: MFCD00149554
Background: An amino-substituted phenylboronic acid used as a reagent for Suzuki-Miyaura cross-coupling. It has been used in the preparation of antivirulence drugs, boronic acid-based beta-lactamase inhibitors, and as a reversible covalent inhibitor of the dopamine transporter in pharmacological research.
Storage: Store at room temperature, under dry conditions.
Cayman Chemical 17 RHDHA Fatty Acids and Deriv
An aspirin-induced DHA metabolite; a precursor to resolvins; inhibits TNF-α-induced IL-1β expression in human glioma cells
Cayman Chemical CAY10448, Purity: ≥98%, CAS: 1177195-52-6, 50 mg
An iodinated nonivamide; a TRPV1 antagonist (IC50 = ~10 nM)
Cayman Chemical 16 SHETE Fatty Acids and Deriv
An inhibitor of proximal tubule ATPase activity; a minor CYP450 metabolite of arachidonic acid
Frontier Specialty Chemicals 100g, 4-(Methoxycarbonyl)phenylboronic acid, 97%, [99768-12-4], M3563 179.97 C8H9BO4
Compound: 4-(Methoxycarbonyl)phenylboronic acid
CAS#: 99768-12-4
MDL#: not listed
Background: A methyl ester-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical and materials science research. The ester group provides a handle for later hydrolysis or amidation.
Storage: Store at room temperature, under dry conditions.
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, Allylboronic acid pinacol ester, 97%, [72824-04-5], A1648 168.05 C9H17BO2
Compound: Allylboronic acid pinacol ester
CAS#: 72824-04-5
MDL#: MFCD00013347
Background: Allylboronic acid pinacol ester is a synthetic specialty chemical useful in the synthesis of pharmaceuticals and specialty organic chemicals. It is commonly used as an allylating reagent in organic synthesis and in transition metal-catalyzed coupling reactions.
Storage: Store at 2-8°C, under dry conditions.
Frontier Specialty Chemicals 25g, 1-Boc-pyrrole-2-boronic acid, 98%, [135884-31-0], B5969 211.02 C9H14BNO4
Compound: 1-Boc-pyrrole-2-boronic acid
CAS#: 135884-31-0
MDL#: MFCD01318939
Background: 1-Boc-pyrrole-2-boronic acid is a protected heteroaryl boronic acid used as a coupling partner in Suzuki-Miyaura cross-coupling reactions. The Boc protecting group allows selective deprotection and further functionalization of the pyrrole ring, making it useful in pharmaceutical synthesis. It has also been applied in the development of sensors for detecting sugars and other biomolecules.
Frontier Specialty Chemicals 5g, 3-Chloropyridine-5-boronic acid, 97%, [872041-85-5], C10087 157.36 C5H5BClNO2
Compound: 3-Chloropyridine-5-boronic acid
CAS#: 872041-85-5
MDL#: MFCD06798243
Background: A chlorinated pyridine boronic acid used in Suzuki-Miyaura cross-coupling reactions. It has been used in the preparation of the PET radioligand [11C]MK-1064 for orexin-2 receptor imaging, the orexin 2 receptor antagonist MK-1064, and ATAD2 bromodomain inhibitors in pharmaceutical research.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, 3-Chloropyridine-5-boronic acid, 97%, [872041-85-5], C10087 157.36 C5H5BClNO2
Compound: 3-Chloropyridine-5-boronic acid
CAS#: 872041-85-5
MDL#: MFCD06798243
Background: A chlorinated pyridine boronic acid used in Suzuki-Miyaura cross-coupling reactions. It has been used in the preparation of the PET radioligand [11C]MK-1064 for orexin-2 receptor imaging, the orexin 2 receptor antagonist MK-1064, and ATAD2 bromodomain inhibitors in pharmaceutical research.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, 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 5g, 2,5-Dimethoxyphenylboronic acid, 97%, [107099-99-0], D6276 181.98 C8H11BO4
Compound: 2,5-Dimethoxyphenylboronic acid
CAS#: 107099-99-0
MDL#: MFCD01318181
Background: 2,5-Dimethoxyphenylboronic acid is an arylboronic acid used as a reactant in Suzuki-Miyaura and Negishi cross-coupling reactions. It is widely utilized in organic synthesis and medicinal chemistry, forming stable complexes with diols that make it useful in pharmaceutical and agrochemical development. It has also been studied for antileishmanial activity through inhibition of protein synthesis and cell division.