Description
Phenylethane Boronic Acid (CAS No. 34420-17-2) is a high-purity boronic acid derivative with the molecular formula C8H11BO2 and IUPAC name 2-phenylethylboronic acid. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. Our product is rigorously tested to ensure ≥95% purity (HPLC/GC) and is supplied as a white to off-white crystalline powder, packaged under inert conditions to prevent degradation. Ideal for pharmaceutical intermediates, materials science, and catalysis research, this compound is characterized by NMR, FTIR, and mass spectrometry for quality assurance. Store in a cool, dry place away from moisture and oxidizing agents.
Properties
- CAS Number: 34420-17-2
- Complexity: 100
- IUPAC Name: 2-phenylethylboronic acid
- InChI: InChI=1S/C8H11BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5,10-11H,6-7H2
- InChI Key: VPRUMANMDWQMNF-UHFFFAOYSA-N
- Exact Mass: 150.0852098
- Molecular Formula: C8H11BO2
- Molecular Weight: 149.98
- SMILES: B(CCC1=CC=CC=C1)(O)O
- Topological: 40.5
- Monoisotopic Mass: 150.0852098
- Synonyms: 34420-17-2, Phenylethane boronic acid, (2-phenylethyl)boronic acid, Boronic acid, (2-phenylethyl)-, DTXSID10188000, DTXCID00110491, 672-926-9, Phenethylboronic acid, 2-phenylethylboronic acid, 2-Phenyl-1-ethylboronic acid, 2-PHENYLETHANEBORONIC ACID, MFCD01631226, PEBA, Phenylethaneboronic acid, Phenethylboronicacid, 2-Phenylethyl-1-boronic acid, 2-Phenylethyl boronic acid, phenethyl boronic acid, (2-phenylethyl)boranediol, 2-phenylethane boronic acid, CHEMBL20461, SCHEMBL129543, B-(2-Phenylethyl)boronic acid, BDBM26142, 5U829XNV85, Boronic acid, B-(2-phenylethyl)-, SBB071100, AKOS005254522, AB09361, AC-5344, CS-W000915, DB01963, PS-9619, NCGC00249462-01, SY014651, DB-016182, NS00073512, P2476, EN300-91342, Q27093058, Z1147227790, Phenethylboronic acid(Contains varying amounts of anhydride), 2-Phenylethylboronic Acid (contains varying amounts of Anhydride)
Application
Phenylethane Boronic Acid serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions for constructing biaryl compounds in pharmaceutical and agrochemical research. It is also employed in the synthesis of boron-containing polymers and advanced materials. Researchers leverage its boronic acid functionality for sensor development and carbohydrate recognition studies.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (66.7%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2A (100%)
- STOT SE 3 (66.7%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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