Description
2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile (CAS No. 214360-47-1) is a high-purity boronic ester derivative with the molecular formula C12H14BNO2. This compound features a benzonitrile moiety tethered to a 5,5-dimethyl-1,3,2-dioxaborinane ring, offering unique reactivity for cross-coupling reactions, particularly in Suzuki-Miyaura couplings. Its rigid cyclic boronate structure enhances stability while maintaining reactivity, making it a valuable intermediate in pharmaceutical synthesis, materials science, and agrochemical research. The product is supplied as a crystalline solid with ≥95% purity (HPLC), rigorously tested for consistency and performance. Ideal for researchers seeking reliable boron-containing building blocks for advanced organic transformations.
Properties
- CAS Number: 214360-47-1
- Complexity: 287
- IUPAC Name: 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile
- InChI: InChI=1S/C12H14BNO2/c1-12(2)8-15-13(16-9-12)11-6-4-3-5-10(11)7-14/h3-6H,8-9H2,1-2H3
- InChI Key: QHAYLPAKZXKQSE-UHFFFAOYSA-N
- Exact Mass: 215.1117589
- Molecular Formula: C12H14BNO2
- Molecular Weight: 215.06
- SMILES: B1(OCC(CO1)(C)C)C2=CC=CC=C2C#N
- Topological: 42.3
- Monoisotopic Mass: 215.1117589
- Synonyms: 214360-47-1, 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile, DTXSID80944019, DTXCID101372374, 801-570-0, 2-Cyanophenylboronic acid, neopentyl ester, Benzonitrile, 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-, MFCD04039011, C12H14BNO2, SCHEMBL4491246, QHAYLPAKZXKQSE-UHFFFAOYSA-N, SBB068308, AKOS004116361, CS-W000900, SS-4616, AC-33892, SY101552, DB-010403, H10175, 2-(2-cyanophenyl)-5,5-dimethyl-1,3,2-dioxaborinane, 2-Cyanophenylboronic acid, neopentyl ester, AldrichCPR, 2-(5,5-dimethyl-1,3,2-dioxaboran-2-yl)benzenecarbonitrile
Application
This boronic ester is widely employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions for biaryl formation in drug discovery. It serves as a versatile precursor for functionalized aromatic compounds in materials science, particularly in OLED and liquid crystal development. The sterically hindered dioxaborinane ring improves selectivity in palladium-catalyzed reactions compared to acyclic analogs.
Safety and Hazards
GHS Hazard Statements
- H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
- H312 (100%): Harmful in contact with skin [Warning Acute toxicity, dermal]
- H315 (50%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (50%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H332 (100%): Harmful if inhaled [Warning Acute toxicity, inhalation]
Precautionary Statements
- P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P321, P330, P332+P317, P337+P317, P362+P364, and P501
Hazard Classes and Categories
- Acute Tox. 4 (100%)
- Acute Tox. 4 (100%)
- Skin Irrit. 2 (50%)
- Eye Irrit. 2 (50%)
- Acute Tox. 4 (100%)
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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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