Description
4-(trans-4-Butylcyclohexyl)phenylboronic acid (CAS: 315220-11-2) is a high-purity boronic acid derivative with the molecular formula C16H25BO2, widely utilized in organic synthesis and pharmaceutical research. This compound features a trans-4-butylcyclohexylphenyl group, making it a valuable intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecular architectures. Its crystalline solid form ensures stability and ease of handling under standard laboratory conditions. Ideal for researchers in medicinal chemistry and material science, this boronic acid derivative is rigorously tested for purity (typically ≥95% by HPLC or NMR) and is available in customizable quantities to meet diverse research needs. Store in a cool, dry place, protected from moisture to maintain optimal performance.
Properties
- CAS Number: 315220-11-2
- Complexity: 241
- IUPAC Name: [4-(4-butylcyclohexyl)phenyl]boronic acid
- InChI: InChI=1S/C16H25BO2/c1-2-3-4-13-5-7-14(8-6-13)15-9-11-16(12-10-15)17(18)19/h9-14,18-19H,2-8H2,1H3
- InChI Key: XAPVHVFVQKPDAJ-UHFFFAOYSA-N
- Exact Mass: 260.1947602
- Molecular Formula: C16H25BO2
- Molecular Weight: 260.2
- SMILES: B(C1=CC=C(C=C1)C2CCC(CC2)CCCC)(O)O
- Topological: 40.5
- Monoisotopic Mass: 260.1947602
- Synonyms: 315220-11-2, 4-(TRANS-4-BUTYLCYCLOHEXYL)PHENYLBORONIC ACID, 4-(4-butylcyclohexyl)phenylboronic acid, [4-(4-Butylcyclohexyl)phenyl]boronic acid, 516510-90-0, (4-(4-Butylcyclohexyl)phenyl)boronic acid, (4-(trans-4-Butylcyclohexyl)phenyl)boronic acid, {4-[(1s,4r)-4-butylcyclohexyl]phenyl}boronic acid, MFCD09750934, SCHEMBL2556952, SCHEMBL29186351, DTXSID40572953, XAPVHVFVQKPDAJ-UHFFFAOYSA-N, AKOS005146051, AKOS015839539, CS-0178337, 4-trans(4-n-Butylcyclohexyl)phenylboronicacid
Application
4-(trans-4-Butylcyclohexyl)phenylboronic acid is primarily employed as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds for pharmaceutical and agrochemical applications. Its structural properties make it suitable for creating liquid crystal materials and advanced organic frameworks. Researchers also leverage its boronic acid functionality in sensor development and carbohydrate recognition studies.
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