Boronic acid derivatives
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Filtered Search Results
Aobchem 2-Chloro-5-cyanophenylboronic acid | ≥97% | CAS 936249-33-1 | C7H5BClNO2 | 10g
2-Chloro-5-cyanophenylboronic acid | ≥97% | CAS 936249-33-1 | C7H5BClNO2 | 10g
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Aobchem 4-Cyano-2-nitrophenylboronic acid | ≥97% | CAS 850568-46-6 | C7H5BN2O4 | 500mg
4-Cyano-2-nitrophenylboronic acid | ≥97% | CAS 850568-46-6 | C7H5BN2O4 | 500mg
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Aobchem Cyclopropylboronic acid pinacol ester | ≥97% | CAS 126689-01-8 | C9H17BO2 | 10g
Cyclopropylboronic acid pinacol ester | ≥97% | CAS 126689-01-8 | C9H17BO2 | 10g
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Aobchem 3-Bromo-5-fluorophenylboronic acid N-butyldiethanolamine ester | ≥97% | CAS 1190989-06-0 | C14H20BBrFNO2 | 10g
3-Bromo-5-fluorophenylboronic acid N-butyldiethanolamine ester | ≥97% | CAS 1190989-06-0 | C14H20BBrFNO2 | 10g
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Sigma Aldrich Fine Chemicals Biosciences Cyclohexylboronic acid >=95% | 4441-56-9 | MFCD01311824 | 10G
Cyclohexylboronic acid >=95% | Purity: >=95% | Mol Wt: 127.98 | 4441-56-9 | MFCD01311824 | 10G
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Frontier Specialty Chemicals 1g, 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: 3-Aminophenylboronic acid monohydrate is an arylboronic acid used as a reagent in Suzuki-Miyaura cross-coupling reactions. It has been used as a boronic acid-based inhibitor of bacterial beta-lactamases, which confer resistance to penicillin and cephem antibiotics. It also serves as a building block for amphiphilic glycopolymers used in glucose-sensing nanoparticles.
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Sigma Aldrich Fine Chemicals Biosciences 1-Methylpyrazole-4-boronic acid pinacol ester 95% | Purity: 95% | Mol Wt: 208.07 | 761446-44-0 | MFCD03789259 | 25G
1-Methylpyrazole-4-boronic acid pinacol ester 95% | Purity: 95% | Mol Wt: 208.07 | 761446-44-0 | MFCD03789259 | 25G
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Sigma Aldrich Fine Chemicals Biosciences 1-Methylpyrazole-4-boronic acid pinacol ester 95% | Purity: 95% | Mol Wt: 208.07 | 761446-44-0 | MFCD03789259 | 1G
1-Methylpyrazole-4-boronic acid pinacol ester 95% | Purity: 95% | Mol Wt: 208.07 | 761446-44-0 | MFCD03789259 | 1G
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Sigma Aldrich Fine Chemicals Biosciences 3-Cyanophenylboronic acid >=95.0% | 150255-96-2 | MFCD01318967 | 5G
3-Cyanophenylboronic acid >=95.0% | Purity: >=95.0% | Mol Wt: 146.94 | 150255-96-2 | MFCD01318967 | 5G
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Frontier Specialty Chemicals 5g, Quinoline-6-boronic acid, 98%, [376581-24-7], B13020 172.976 C9H8BNO2
Compound: Quinoline-6-boronic acid
CAS#: 376581-24-7
MDL#: not listed
Background: A quinoline boronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. It provides a convenient means to introduce a substituted quinoline scaffold into drug candidate synthesis.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 1g, 3-Fluoro-5-methoxyphenylboronic acid, 98%, [609807-25-2], F2100 169.95 C7H8BFO3
Compound: 3-Fluoro-5-methoxyphenylboronic acid
CAS#: 609807-25-2
MDL#: MFCD07366780
Background: 3-Fluoro-5-methoxyphenylboronic acid is used for proteomics research and forms stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. It is used in the development of pharmaceuticals, agrochemicals, and advanced materials, as well as in biosensing and diagnostic applications due to its selective binding to specific biomolecules.
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Frontier Specialty Chemicals 5g, 1-Methyl-1H-pyrazole-4-boronic acid pinacol ester, 97%, [761446-44-0], M10073 208.07 C10H17BN2O2
Compound: 1-Methyl-1H-pyrazole-4-boronic acid pinacol ester
CAS#: 761446-44-0
MDL#: MFCD03789259
Background: A methylated pyrazole boronic ester used as a reagent for Suzuki-Miyaura cross-coupling and transesterification reactions. It serves as an alternative to the free boronic acid in palladium-catalyzed coupling chemistry used in pharmaceutical research.
Storage: Store at room temperature, under dry conditions.
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Frontier Specialty Chemicals 1g, (2-Methylpropyl)boronic acid, 97%, [84110-40-7], I7111 101.94 C4H11BO2
Compound: (2-Methylpropyl)boronic acid
CAS#: 84110-40-7
MDL#: MFCD00134156
Background: (2-Methylpropyl)boronic acid, also known as isobutylboronic acid, has been used to synthesize potent and selective dipeptidyl boronic acid proteasome inhibitors studied as therapeutics for cancer and inflammatory diseases, and in the preparation of isocoumarin analogs as gamma-secretase cleavage inhibitors. It is also used broadly in Suzuki-Miyaura reactions for the synthesis of complex pharmaceutical and agrochemical molecules.
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Frontier Specialty Chemicals 1g, 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.
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Frontier Specialty Chemicals 25g, 4-(N-Methylaminocarbonyl)phenylboronic acid, 98%, [121177-82-0], M10870 178.981 C8H10BNO3
Compound: 4-(N-Methylaminocarbonyl)phenylboronic acid
CAS#: 121177-82-0
MDL#: not listed
Background: A secondary amide-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in pharmaceutical research. The amide N-H offers a site for hydrogen bonding, useful for tuning the physicochemical properties of downstream coupled products.
Storage: Store at room temperature, under dry conditions.
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