4-n-pentylbenzene boronic acid

Price on application

4-n-pentylbenzene boronic acid – Suzuki-Miyaura coupling partner, C11H17BO2, CAS 121219-12-3. Price on application.

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SKU: KC1032 Category:
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3D model (4-Pentylphenyl)boronic acid, CAS 121219-12-3, molecular formula C11H17BO2, molar mass 192.06 g/mol
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Description

4-n-pentylbenzene boronic acid is an arylboronic acid built on a benzene core, carrying a pentyl chain. It serves as the nucleophilic partner in Suzuki-Miyaura cross-coupling, transferring its aryl group to a palladium centre under basic conditions.

Key data

  • Catalogue code: KC1032
  • CAS number: 121219-12-3
  • Molecular formula: C11H17BO2
  • Molecular weight: 192.06 g/mol
  • Category: Boronic Acids

What the substitution pattern does

The pentyl chain places this compound at n=5 in its homologous series. Chain length is not a cosmetic variable here: each added methylene lowers the melting point unevenly and shifts the balance between nematic and smectic order, because an odd-numbered chain sets its terminal bond at a different angle to the molecular long axis than an even one. Homologues therefore alternate in behaviour rather than trending smoothly, and an odd-numbered member frequently outperforms both of its neighbours for a given formulation.

Typical applications

  • Suzuki-Miyaura cross-coupling with aryl halides and triflates
  • construction of biphenyl and terphenyl cores for liquid crystal mixtures
  • late-stage arylation in medicinal and agrochemical discovery routes
  • Chan-Lam C-N and C-O couplings under copper catalysis
  • conversion to the matching potassium trifluoroborate for storage-stable stock

Ordering

This compound is supplied to order. Pricing depends on quantity and on the specification you need, so it is quoted rather than listed – send an enquiry stating the quantity and any purity or analytical requirement, and you will receive a written quotation.

Please quote CAS 121219-12-3 or catalogue code KC1032 when enquiring, so that the correct isomer is supplied.

Handling and documentation

Supplied for laboratory and industrial use by trained personnel only. Not for use as a medicine, food, cosmetic or biocide, and not for administration to humans or animals. Safety documentation is issued with the order; this page is not a source of hazard information.

Additional information

Catalogue code

KC1032

CAS number

121219-12-3

Molecular formula

C11H17BO2

Molecular weight

192.06 g/mol

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Extended Bibliography (5)

  1. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "Unified Strategy for the Concise Total Syntheses of All Six 3OAcyl Quercitrins Based on Regioselective Acylation Catalyzed by Boronic Acid.". https://doi.org/10.1021/acs.joc.4c02659.s001. link [accessed: 2026-08-25] CC0 (metadata)
  2. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "Visualization of Boronic Acid Containing Pharmaceuticals in Live Tumor Cells Using a Fluorescent Boronic Acid Sensor.". https://doi.org/10.1021/acssensors.6b00522.s001. link [accessed: 2026-08-25] CC0 (metadata)
  3. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "Which Is Reactive in Alkaline Solution, Boronate Ion or Boronic Acid? Kinetic Evidence for Reactive Trigonal Boronic Acid in an Alkaline Solution.". https://doi.org/10.1021/ic0615372.s001. link [accessed: 2026-08-25] CC0 (metadata)
  4. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "Boronic Acid Pairs for Sequential Bioconjugation.". https://doi.org/10.1021/acs.orglett.1c01624.s001. link [accessed: 2026-08-25] CC0 (metadata)
  5. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "Phosphonic Acid-Boronic Acid Anhydrides Demonstrate Class AD Lactamase Inhibition.". https://doi.org/10.1021/acs.joc.5c02782.s001. link [accessed: 2026-08-25] CC0 (metadata)
Data from PubChemSource: PubChem (NIH) · ChEMBL
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