Trimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silane - Names and Identifiers
Name | 4-Trimethylsilylbenzeneboronic acid pinacol ester
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Synonyms | 4-TriMethylsilylphenylboronic acid pinacol ester 4-Trimethylsilylbenzeneboronic acid pinacol ester 4-TRIMETHYLSILYLBENZENEBORONIC ACID PINACOL ESTER TRIMETHYL(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL) 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)trimethylsilylbenzene Trimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silane 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(trimethylsilyl)phenyl]-
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CAS | 1186026-67-4
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Trimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silane - Physico-chemical Properties
Molecular Formula | C15H25BO2Si
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Molar Mass | 276.25 |
Density | 0.95±0.1 g/cm3(Predicted) |
Boling Point | 335.4±25.0 °C(Predicted) |
Storage Condition | 2-8°C |
Sensitive | IRRITANT |
MDL | MFCD09037796 |
Trimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silane - Introduction
4-Trimethylsilylphenylborate is an organic compound with the following properties:
1. Appearance: 4-trimethylsilyl phenylboronic acid ester is generally colorless or light yellow liquid.
2. melting point and boiling point: its melting point is about -50 ℃, boiling point is about 200 ℃.
3. Solubility: 4-trimethylsilyl phenylboronic acid ester is soluble in a variety of organic solvents, such as ethanol, toluene, etc.
The main uses of 4-trimethylsilylphenylboronic acid pinanol ester include the following aspects:
1. Chemical synthesis: As a catalyst or reagent in organic synthesis, it can participate in important organic reactions such as carbon-hydrogen bond activation and carbonylation reactions.
2. Materials science: It can be used to synthesize inorganic-organic hybrid materials such as polymer materials and metal-organic frameworks (MOF), and has potential applications in regulating structure and function.
3. Biomedicine: Due to its low toxicity to organisms and water-soluble properties, it can be used in biomedical fields such as drug delivery, biomarkers, and cell imaging.
The preparation of 4-trimethylsilylphenylboronic acid pinazol ester is usually carried out by chemical synthesis, and the specific steps and conditions can be carried out according to the methods in the literature or patents.
regarding safety information, there is no special risk report for 4-trimethylsilylphenylboronic acid nitinol ester at present, but the following points still need to be noted:
1. avoid inhalation and skin contact: in operation and use should wear appropriate protective measures, such as wear gloves, goggles and protective clothing.
2. avoid swallowing: inedible, eat or swallow the case should be immediately sought medical attention.
3. storage and transportation: storage should keep sealed, avoid contact with oxygen, acid and alkali. Be careful to avoid violent vibration and high temperature during transportation.
When using and handling this compound, good laboratory practices and operating procedures should be followed, and relevant safety guidelines should be followed. It is best to operate under the guidance of a professional.
Please note that the above only provides a general description of 4-trimethylsilylphenylboronic acid ester, and specific properties, uses and safety information need to be studied and understood in detail.
Last Update:2024-04-10 22:41:03