Boronic acid derivatives
![Frontier Specialty Chemicals 25g, Cyclohexylboronic acid pinacol ester, >95%, [87100-15-0], C1155 210.12 C12H23BO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 25g, 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 1g, 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.
Frontier Specialty Chemicals 1g, 2-Methylprop-1-enylboronic acid pinacol ester, 98%, [126689-00-7], M11191 182.068 C10H19BO2
Compound: 2-Methylprop-1-enylboronic acid pinacol ester
CAS#: 126689-00-7
MDL#: not listed
Background: A branched alkenylboronic ester used as a Suzuki-Miyaura coupling partner in organic synthesis. It provides a convenient means to introduce an isobutenyl group into pharmaceutical and materials science building blocks.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 5g, 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.
Aobchem 3-Ethoxy-5-fluorophenylboronic acid | ≥97% | CAS 850589-53-6 | C8H10BFO3 | 10g
3-Ethoxy-5-fluorophenylboronic acid | ≥97% | CAS 850589-53-6 | C8H10BFO3 | 10g
Aobchem 3-Bromo-4-fluorophenylboronic acid | ≥97% | CAS 1092533-91-9 | C6H5BBrFO2 | 5g
3-Bromo-4-fluorophenylboronic acid | ≥97% | CAS 1092533-91-9 | C6H5BBrFO2 | 5g
Aobchem 3-Cyano-2-fluorophenylboronic acid | ≥97% | CAS 957121-05-0 | C7H5BFNO2 | 5g
3-Cyano-2-fluorophenylboronic acid | ≥97% | CAS 957121-05-0 | C7H5BFNO2 | 5g
Aobchem 4-Bromo-3-carboxyphenylboronic acid | ≥97% | CAS 1451393-32-0 | C7H6BBrO4 | 500mg
4-Bromo-3-carboxyphenylboronic acid | ≥97% | CAS 1451393-32-0 | C7H6BBrO4 | 500mg
Aobchem 4-Bromo-2-methoxyphenylboronic acid | ≥97% | CAS 889849-21-2 | C7H8BBrO3 | 500mg
4-Bromo-2-methoxyphenylboronic acid | ≥97% | CAS 889849-21-2 | C7H8BBrO3 | 500mg
Aobchem 4-Amino-2-fluorophenylboronic acid pinacol ester | ≥95% | CAS 819057-45-9 | C12H17BFNO2 | 10g
4-Amino-2-fluorophenylboronic acid pinacol ester | ≥95% | CAS 819057-45-9 | C12H17BFNO2 | 10g
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.
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.
Frontier Specialty Chemicals 1g, 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.
Frontier Specialty Chemicals 1g, 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.
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.