3-[(2-methoxyethoxy)methyl]phenylboronic acid
(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid
CAS: 1256358-61-8
Molecular Formula: C10H15BO4
3-[(2-methoxyethoxy)methyl]phenylboronic acid - Names and Identifiers
3-[(2-methoxyethoxy)methyl]phenylboronic acid - Physico-chemical Properties
| Molecular Formula | C10H15BO4 |
| Molar Mass | 210.03 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD14687274 |
3-[(2-methoxyethoxy)methyl]phenylboronic acid - Introduction
(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is an organic compound with the chemical formula C11H17BO5. It is a white solid, soluble in common organic solvents such as chloroform, methanol and dimethylformamide.
(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is often used as a reagent in organic synthesis. It can be used as a boronic acid derivative to participate in coupling reactions, such as Suzuki-Miyaura reaction, Stille reaction and Negishi reaction. These reactions can be used to construct aromatic and heterocyclic compounds. In addition, it can also be used to synthesize drugs, natural products and other organic compounds.
The method for preparing (3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is generally obtained by reacting p-hydroxybenzaldehyde with triphenylphosphine hydrochloride in the presence of boric acid.
Regarding safety information,(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is generally less toxic and dangerous under normal conditions of use. However, it is still necessary to follow general laboratory safety practices, such as wearing protective gloves, glasses and laboratory atmosphere protection equipment. Avoid inhalation, skin contact and ingestion. If you take it by mistake or accidentally touch it, please wash it in time and seek medical assistance.
(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is often used as a reagent in organic synthesis. It can be used as a boronic acid derivative to participate in coupling reactions, such as Suzuki-Miyaura reaction, Stille reaction and Negishi reaction. These reactions can be used to construct aromatic and heterocyclic compounds. In addition, it can also be used to synthesize drugs, natural products and other organic compounds.
The method for preparing (3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is generally obtained by reacting p-hydroxybenzaldehyde with triphenylphosphine hydrochloride in the presence of boric acid.
Regarding safety information,(3-((2-Methoxyethoxy)methyl)phenyl)boronic acid is generally less toxic and dangerous under normal conditions of use. However, it is still necessary to follow general laboratory safety practices, such as wearing protective gloves, glasses and laboratory atmosphere protection equipment. Avoid inhalation, skin contact and ingestion. If you take it by mistake or accidentally touch it, please wash it in time and seek medical assistance.
Last Update：2024-04-09 20:13:35
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