1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine - Names and Identifiers
| Name | 3-Aminomethylphenylboronicacidpinacolester
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| Synonyms | 3-Aminomethylphenylboronicacidpinacolester
(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine
Benzenemethanamine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine
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| CAS | 269410-09-5
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1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine - Physico-chemical Properties
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine - Upstream Downstream Industry
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine - Introduction
It is also known as an organic compound. Its chemical structure contains a benzene ring, a nitrogen-containing amino group and a boronic acid group. The compound has some of the following properties:
1. Appearance: Colorless or slightly yellow crystalline solid.
2. Solubility: Easy to dissolve in common organic solvents (such as ethanol, dimethylformamide, etc.).
3. Stability: relatively stable at room temperature, but may react under the conditions of strong oxidants and strong acids.
This compound has certain application value in chemical research and synthesis, mainly used in the following aspects:
1. Organic synthesis: As an important reagent for aromatic amines, it can be used to construct C- C bonds and C- N bonds, and participate in reactions similar to Suzuki coupling reactions and reduced amines.
2. Chemical sensor: Due to the boronic acid group, the compound can form a stable alcohol ester complex with certain molecules, which can be used as a chemical sensor for detecting molecules.
3. Drug development: the compound can be used in the design and synthesis of drugs, as a part of the molecular structure of the building block.
The method of preparing the compound is mainly obtained by the method of organic synthetic chemistry, and the general steps are as follows:
1. To obtain the required raw materials (such as pinacol, 3-amino methyl benzene boric acid, etc.).
2. The reaction is carried out in an appropriate solvent and the reaction conditions (such as temperature, pH value, etc.) are controlled.
3. Purify and separate the reaction product using appropriate techniques (e. G., crystallization, column chromatography, etc.).
For safety information, please note the following when handling this compound:
1. Wear appropriate personal protective equipment, including lab coats, goggles and gloves.
2. Avoid inhaling the dust or solution of the compound to avoid irritation or toxic reactions.
3. During the operation, try to avoid contact with skin. If contact occurs, rinse with plenty of water immediately and seek medical assistance.
4. Storage should be sealed container, avoid contact with oxidants and acidic substances, stored in a dry, ventilated place.
Last Update：2024-04-09 21:21:28