Boronic acid derivatives
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Filtered Search Results
Aobchem 2-Bromo-5-fluorophenylboronic acid | ≥97% | CAS 959996-48-6 | C6H5BBrFO2 | 25g
2-Bromo-5-fluorophenylboronic acid | ≥97% | CAS 959996-48-6 | C6H5BBrFO2 | 25g
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Aobchem 2 4-Dimethoxyphenylboronic acid pinacol ester | ≥97% | CAS 214360-69-7 | C14H21BO4 | 10g
2 4-Dimethoxyphenylboronic acid pinacol ester | ≥97% | CAS 214360-69-7 | C14H21BO4 | 10g
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Aobchem 2-Fluoro-5-nitrophenylboronic acid | ≥97% | CAS 819849-20-2 | C6H5BFNO4 | 10g
2-Fluoro-5-nitrophenylboronic acid | ≥97% | CAS 819849-20-2 | C6H5BFNO4 | 10g
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Aobchem 2-Bromo-5-methoxyphenylboronic acid | ≥97% | CAS 89694-44-0 | C7H8BBrO3 | 25g
2-Bromo-5-methoxyphenylboronic acid | ≥97% | CAS 89694-44-0 | C7H8BBrO3 | 25g
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Aobchem 3-Bromo-5-methoxyphenylboronic acid | ≥97% | CAS 849062-12-0 | C7H8BBrO3 | 5g
3-Bromo-5-methoxyphenylboronic acid | ≥97% | CAS 849062-12-0 | C7H8BBrO3 | 5g
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Aobchem 2-Chloro-5-fluorophenylboronic acid | ≥97% | CAS 444666-39-1 | C6H5BClFO2 | 25g
2-Chloro-5-fluorophenylboronic acid | ≥97% | CAS 444666-39-1 | C6H5BClFO2 | 25g
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Aobchem 5-Acetyl-2-fluorophenylboronic acid | ≥97% | CAS 870777-29-0 | C8H8BFO3 | 25g
5-Acetyl-2-fluorophenylboronic acid | ≥97% | CAS 870777-29-0 | C8H8BFO3 | 25g
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Aobchem 2-Chloro-3-fluorophenylboronic acid | ≥95% | CAS 871329-52-1 | C6H5BClFO2 | 25g
2-Chloro-3-fluorophenylboronic acid | ≥95% | CAS 871329-52-1 | C6H5BClFO2 | 25g
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Aobchem 2-Chloro-3-fluorophenylboronic acid | ≥95% | CAS 871329-52-1 | C6H5BClFO2 | 10g
2-Chloro-3-fluorophenylboronic acid | ≥95% | CAS 871329-52-1 | C6H5BClFO2 | 10g
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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.
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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.
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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.
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Frontier Specialty Chemicals 5g, 4-(Methoxycarbonyl)phenylboronic acid, 97%, [99768-12-4], M3563 179.97 C8H9BO4
Compound: 4-(Methoxycarbonyl)phenylboronic acid
CAS#: 99768-12-4
MDL#: MFCD01632203
Background: 4-(Methoxycarbonyl)phenylboronic acid is an arylboronic acid used as a key intermediate in pharmaceutical synthesis. It participates in Suzuki cross-coupling reactions to form carbon-carbon bonds for the construction of biaryl scaffolds. It has been used in the synthesis of HIV-1 maturation inhibitors and other drug candidates.
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Frontier Specialty Chemicals 1g, Pyridine-3-boronic acid, 95%, [1692-25-7], P5775 122.92 C5H6BNO2
Compound: Pyridine-3-boronic acid
CAS#: 1692-25-7
MDL#: MFCD00674177
Background: Pyridine-3-boronic acid is a heteroaryl boronic acid used as a building block in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds containing a pyridine ring. It has been applied in phosphine-free and regioselective coupling methods, including tandem coupling-annulation sequences to build fused nitrogen heterocycles. It also supplies the 3-pyridyl unit used in the synthesis of the Bcr-Abl tyrosine-kinase inhibitor nilotinib.
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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.
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