4,4,5,5-Tetramethyl-2-octyl-1,3,2-dioxaborolane
Octylboronic acid
CAS: 66217-56-9
Molecular Formula: C14H29BO2
4,4,5,5-Tetramethyl-2-octyl-1,3,2-dioxaborolane - Names and Identifiers
4,4,5,5-Tetramethyl-2-octyl-1,3,2-dioxaborolane - Physico-chemical Properties
| Molecular Formula | C14H29BO2 |
| Molar Mass | 240.19 |
4,4,5,5-Tetramethyl-2-octyl-1,3,2-dioxaborolane - Upstream Downstream Industry
| Downstream Products | 1-Phenylnonane |
4,4,5,5-Tetramethyl-2-octyl-1,3,2-dioxaborolane - Introduction
Octylboronic acid(Octylboronic acid), also known as octyl borate, is an organoboron compound. The following is an introduction to the nature, use, formulation and safety information of Octylboronic acid:
Nature:
-Appearance: Octylboronic acid is usually a colorless or light yellow liquid.
-Solubility: Octylboronic acid can be dissolved in many organic solvents, such as ether, methylene chloride and methanol.
-Stability: Octylboronic acid is relatively stable to air and water.
Use:
-Organic synthesis: Octylboronic acid is an important organic synthesis reagent, commonly used in Suzuki coupling reaction. It can be reacted with organic halides or organic sulfonates to form the corresponding aromatic compounds.
-Chemical research: Octylboronic acid can be used as catalysts and ligands for organic synthesis reactions.
Preparation Method:
- Octylboronic acid can be generated under acidic conditions by the reaction of octyl ether and triphenylborane.
Safety Information:
- Octylboronic acid is generally a low-toxic substance, but still need to pay attention to safe operation.
-When in use, wear appropriate protective gloves and goggles to avoid contact with skin and eyes.
-Avoid inhaling or ingesting substances and ensure that you operate in a well-ventilated place.
-In the event of contact or ingestion, a physician should be immediately requested for assistance, along with the details on the package.
Nature:
-Appearance: Octylboronic acid is usually a colorless or light yellow liquid.
-Solubility: Octylboronic acid can be dissolved in many organic solvents, such as ether, methylene chloride and methanol.
-Stability: Octylboronic acid is relatively stable to air and water.
Use:
-Organic synthesis: Octylboronic acid is an important organic synthesis reagent, commonly used in Suzuki coupling reaction. It can be reacted with organic halides or organic sulfonates to form the corresponding aromatic compounds.
-Chemical research: Octylboronic acid can be used as catalysts and ligands for organic synthesis reactions.
Preparation Method:
- Octylboronic acid can be generated under acidic conditions by the reaction of octyl ether and triphenylborane.
Safety Information:
- Octylboronic acid is generally a low-toxic substance, but still need to pay attention to safe operation.
-When in use, wear appropriate protective gloves and goggles to avoid contact with skin and eyes.
-Avoid inhaling or ingesting substances and ensure that you operate in a well-ventilated place.
-In the event of contact or ingestion, a physician should be immediately requested for assistance, along with the details on the package.
Last Update：2024-04-09 02:00:50
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