Boronic acid derivatives
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Filtered Search Results
Frontier Specialty Chemicals 1g, 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.
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Frontier Specialty Chemicals 1g, 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.
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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.
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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.
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Frontier Specialty Chemicals 5g, 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.
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Frontier Specialty Chemicals 1g, 2-Isopropenyl boronic acid pinacol ester, 98%, [126726-62-3], I10296 168.041 C9H17BO2
Compound: 2-Isopropenyl boronic acid pinacol ester
CAS#: 126726-62-3
MDL#: not listed
Background: An isopropenyl-substituted pinacol boronate used as a Suzuki-Miyaura coupling partner in organic synthesis. It is a versatile reagent for introducing an isopropenyl group into pharmaceutical and materials science building blocks.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 25g, 3-Fluoro-5-methoxyphenylboronic acid, 98%, [609807-25-2], F2100 169.95 C7H8BFO3
Compound: 3-Fluoro-5-methoxyphenylboronic acid
CAS#: 609807-25-2
MDL#: not listed
Background: A fluorinated, methoxylated phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. It is a common building block for constructing substituted biaryl scaffolds in medicinal chemistry.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 25g, 2-Isopropenyl boronic acid pinacol ester, 98%, [126726-62-3], I10296 168.041 C9H17BO2
Compound: 2-Isopropenyl boronic acid pinacol ester
CAS#: 126726-62-3
MDL#: not listed
Background: An isopropenyl-substituted pinacol boronate used as a Suzuki-Miyaura coupling partner in organic synthesis. It is a versatile reagent for introducing an isopropenyl group into pharmaceutical and materials science building blocks.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 25g, (2-Methylpropyl)boronic acid, 97%, [84110-40-7], I7111 101.94 C4H11BO2
Compound: (2-Methylpropyl)boronic acid
CAS#: 84110-40-7
MDL#: not listed
Background: An isobutylboronic acid used as a Suzuki-Miyaura coupling partner in organic synthesis. It provides a convenient means to introduce a branched isobutyl group into pharmaceutical and agrochemical building blocks.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 25g, 2-(Trifluoromethyl)pyridine-5-boronic acid, 97%, [868662-36-6], T10181 190.92 C6H5BF3NO2
Compound: 2-(Trifluoromethyl)pyridine-5-boronic acid
CAS#: 868662-36-6
MDL#: MFCD07375381
Background: A trifluoromethylated pyridine boronic acid valued for its ability to participate in Suzuki-Miyaura coupling reactions, serving as an essential building block for pharmaceuticals, agrochemicals, and materials science research. The trifluoromethyl group enhances lipophilicity, improving the bioavailability of resulting drug candidates.
Storage: Store at room temperature, under dry conditions.
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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.
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Frontier Specialty Chemicals 5g, 4-(N-Boc-aminomethyl)phenylboronic acid, 97%, [489446-42-6], A1231 251.09 C12H18BNO4
Compound: 4-(N-Boc-aminomethyl)phenylboronic acid
CAS#: 489446-42-6
MDL#: MFCD04115637
Background: 4-(N-Boc-aminomethyl)phenylboronic acid is a Boc-protected phenylboronic acid used for proteomics research and as a key building block in pharmaceutical and agrochemical synthesis. Its boronic acid functionality supports Suzuki-Miyaura cross-coupling reactions, while the protected amino group enables selective manipulation of specific sites within a molecule during multi-step synthesis.
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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.
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Frontier Specialty Chemicals 1g, 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.
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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.
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