Boronic acid, B-[3-[[(1,1-dimethylethyl)methylamino]sulfonyl]phenyl]-
(3-(N-(tert-Butyl)-N-methylsulfamoyl)-phenyl)boronic acid
CAS: 1217501-22-8
Molecular Formula: C11H18BNO4S
Boronic acid, B-[3-[[(1,1-dimethylethyl)methylamino]sulfonyl]phenyl]- - Names and Identifiers
Boronic acid, B-[3-[[(1,1-dimethylethyl)methylamino]sulfonyl]phenyl]- - Physico-chemical Properties
| Molecular Formula | C11H18BNO4S |
| Molar Mass | 271.14 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD12756419 |
Boronic acid, B-[3-[[(1,1-dimethylethyl)methylamino]sulfonyl]phenyl]- - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36 - Irritating to the eyes |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
Boronic acid, B-[3-[[(1,1-dimethylethyl)methylamino]sulfonyl]phenyl]- - Introduction
(3-(N-(tert-Butyl)-N-methylsulfamoyl)-phenyl)boronic acid is an organic compound with the chemical formula C14H21BN2O4S. It is a white to off-white crystalline solid.
This compound is commonly used as a reagent in organic synthesis and has important applications in metal-catalyzed reactions, alkene carbonylation and coupling reactions. It can be used as a substitute for amino hydroxy acid template, an intermediate for natural drug synthesis and a precursor for fluorescent probes.
The preparation of (3-(N-(tert-Butyl)-N-methylsulfamoyl)-phenyl)boronic acid is usually obtained by reacting p-toluenesulfonamide with Bowlerite reagent.
Regarding safety information, caution is required for the use of any chemical. This compound may be a potential risk to health and the environment, so appropriate safety measures such as wearing protective gloves, goggles and protective clothing are required during use. At the same time, the relevant chemical storage, handling and transportation regulations should be observed. For laboratory use, refer to the relevant Safety Data Sheet (SDS) for more detailed safety information.
This compound is commonly used as a reagent in organic synthesis and has important applications in metal-catalyzed reactions, alkene carbonylation and coupling reactions. It can be used as a substitute for amino hydroxy acid template, an intermediate for natural drug synthesis and a precursor for fluorescent probes.
The preparation of (3-(N-(tert-Butyl)-N-methylsulfamoyl)-phenyl)boronic acid is usually obtained by reacting p-toluenesulfonamide with Bowlerite reagent.
Regarding safety information, caution is required for the use of any chemical. This compound may be a potential risk to health and the environment, so appropriate safety measures such as wearing protective gloves, goggles and protective clothing are required during use. At the same time, the relevant chemical storage, handling and transportation regulations should be observed. For laboratory use, refer to the relevant Safety Data Sheet (SDS) for more detailed safety information.
Last Update：2024-04-09 21:11:58
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