Boronic acid derivatives
Aobchem Isoquinoline-5-boronic acid | ≥97% | CAS 371766-08-4 | C9H8BNO2 | 5g
Isoquinoline-5-boronic acid | ≥97% | CAS 371766-08-4 | C9H8BNO2 | 5g
Aobchem 2-Ethoxy-4-fluorophenylboronic acid | ≥97% | CAS 480438-58-2 | C8H10BFO3 | 25g
2-Ethoxy-4-fluorophenylboronic acid | ≥97% | CAS 480438-58-2 | C8H10BFO3 | 25g
Aobchem 4-Methyl-3-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1072945-06-2 | C13H18BNO4 | 10g
4-Methyl-3-nitrophenylboronic acid pinacol ester | ≥97% | CAS 1072945-06-2 | C13H18BNO4 | 10g
Aobchem 4-Ethoxy-3-fluorophenylboronic acid | ≥97% | CAS 279263-10-4 | C8H10BFO3 | 25g
4-Ethoxy-3-fluorophenylboronic acid | ≥97% | CAS 279263-10-4 | C8H10BFO3 | 25g
Aobchem 6-Ethoxy-2-naphthaleneboronic acid | ≥97% | CAS 352525-98-5 | C12H13BO3 | 25g
6-Ethoxy-2-naphthaleneboronic acid | ≥97% | CAS 352525-98-5 | C12H13BO3 | 25g
Aobchem 3-(2-Bromophenylcarbamoyl)phenylboronic acid | ≥97% | CAS 874288-30-9 | C13H11BBrNO3 | 5g
3-(2-Bromophenylcarbamoyl)phenylboronic acid | ≥97% | CAS 874288-30-9 | C13H11BBrNO3 | 5g
eMolecules 137401-45-7 | 2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid | ChemScene | MFCD09835539 | 247.247 | C10H17NO6 | 97.000 | CCOC(=O)C(NC(=O)OC(C)(C)C)C(O)=O | 25g | 572245531
2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid | ChemScene | 137401-45-7 | MFCD09835539 | 247.247 | C10H17NO6 | 97.000 | CCOC(=O)C(NC(=O)OC(C)(C)C)C(O)=O | 25g | 572245531
![Frontier Specialty Chemicals 5g, Quinoline-6-boronic acid, 98%, [376581-24-7], B13020 172.976 C9H8BNO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
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 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.
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.
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.
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.
Cayman Chemical CAY10462, Purity: ≥98%, CAS: 502656-68-0, 1 mg
A selective inhibitor of the 20-HETE synthase CYP4A11 (IC50 = 8.8 nM in human renal microsomes); 200-fold less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes