Description

2-(Cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a high-purity boronic ester compound widely used in organic synthesis, pharmaceutical research, and material science. With the molecular formula C₁₂H₂₁BO₂ and CAS number 141091-37-4, this reagent is an essential building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. The pinacol ester group enhances stability, making it ideal for handling and storage under standard laboratory conditions. This product is rigorously tested for quality, ensuring optimal performance in catalytic applications, ligand synthesis, and advanced material development. Packaged under inert conditions to prevent degradation, it is available in various quantities to meet both research and industrial-scale demands.

Properties

• CAS Number: 141091-37-4
• Complexity: 265
• IUPAC Name: 2-(cyclohexen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• InChI: InChI=1S/C12H21BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h8H,5-7,9H2,1-4H3
• InChI Key: QNZFUMVTUFOLRT-UHFFFAOYSA-N
• Exact Mass: 208.1634601
• Molecular Formula: C12H21BO2
• Molecular Weight: 208.11
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CCCCC2
• Topological: 18.5
• Monoisotopic Mass: 208.1634601
• Synonyms: 141091-37-4, 2-(cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, DTXSID80448820, DTXCID80399641, 640-223-6, Cyclohexene-1-boronic acid pinacol ester, 1-Cyclohexen-yl-boronic acid pinacol ester, 1-Cyclohexen-1-yl-boronic acid pinacol ester, Cyclohexen-1-ylboronic acid, pinacol ester, 1,3,2-DIOXABOROLANE, 2-(1-CYCLOHEXEN-1-YL)-4,4,5,5-TETRAMETHYL-, 1-Cyclohexeneboronic Acid Pinacol Ester, MFCD05663845, 2-(1-cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-(cyclohexen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-cyclohexenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-(1-CYCLOHEXEN-1-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE, 1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexene, 1-cyclohexenylboronic acid pinacol ester, Cyclohexen-1-yl-boronic acid pinacol ester, SCHEMBL422542, C12H21BO2, QNZFUMVTUFOLRT-UHFFFAOYSA-N, BCP12569, cyclohexenylboronic acid pinacol ester, AKOS000283810, AB21933, CS-W007746, GS-6455, HY-W007746, 1-cyclohexenyl boronic acid pinacol ester, PD200192, SY007878, 1-cyclohexen-1-ylboronic acid pinacol ester, DB-009174, C2707, 1-(1-Cyclohexenyl)boronic Acid Pinacol Ester, Cyclohex-1-ene-1-boronic acid, pinacol ester, EN300-98764, CYCLOHEX-1-EN-1-YLBORONIC ACID PINACOL ESTER, Z1318515141, 2-cyclohex-1-enyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane, 2-cyclohexen-1-yl-4,4,5,5-tetramethyl-[1.3.2]dioxaborolane, 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen cyclohexenylboronate, 2-cyclohex-1-en-1-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

This compound is primarily employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex organic molecules for pharmaceuticals and agrochemicals. It is also utilized in the preparation of boron-containing polymers and advanced materials with tailored electronic properties. Researchers leverage its stability and reactivity in medicinal chemistry for drug discovery and development.

Safety and Hazards

GHS Hazard Statements

• H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]
• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (50%)
• Skin Irrit. 2 (100%)
• Eye Irrit. 2A (100%)
• STOT SE 3 (100%)

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.