1217501-49-9
(4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid
CAS: 1217501-49-9
Molecular Formula: C10H14BNO4S
1217501-49-9 - Names and Identifiers
1217501-49-9 - Physico-chemical Properties
| Molecular Formula | C10H14BNO4S |
| Molar Mass | 255.1 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD13195670 |
1217501-49-9 - Introduction
(4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is an organic compound with the chemical formula C12H16BNO4S. The following is a description of its nature, use, formulation and safety information:
Nature:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is a white solid, soluble in organic solvents such as dichloromethane and ethanol, but less soluble in water.
-It is acidic and can participate in organic synthesis reactions, such as reacting with organotin compounds to generate complexes bonded to organotin.
Use:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is an organic boron compound, widely used in coupling reactions in organic synthesis reactions, where tin or boron is part of the substrate to form a carbon-carbon bond.
-It is often used in the field of pharmaceutical research for the synthesis of novel molecules and drug candidate compounds.
-It is also often used in the synthesis of organic optoelectronic materials and coordination chemistry.
Preparation Method:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid can be prepared by a variety of synthetic methods. The common method is to react boric acid with the corresponding aromatic amine and cyclopropene methanesulfonic acid.
Safety Information:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is relatively safe under correct handling and storage conditions. However, care should be taken to avoid direct contact with skin and eyes to avoid irritation.
-Wear appropriate personal protective equipment, such as lab gloves and safety glasses, to avoid inhaling dust or solution into the mouth or food.
-The handling and storage should follow the relevant safety procedures, and manage and dispose in accordance with local laws and regulations. Under improper use and disposal, may have adverse effects on the environment. Therefore, it is recommended to follow the correct laboratory safety operation guidelines.
Nature:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is a white solid, soluble in organic solvents such as dichloromethane and ethanol, but less soluble in water.
-It is acidic and can participate in organic synthesis reactions, such as reacting with organotin compounds to generate complexes bonded to organotin.
Use:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is an organic boron compound, widely used in coupling reactions in organic synthesis reactions, where tin or boron is part of the substrate to form a carbon-carbon bond.
-It is often used in the field of pharmaceutical research for the synthesis of novel molecules and drug candidate compounds.
-It is also often used in the synthesis of organic optoelectronic materials and coordination chemistry.
Preparation Method:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid can be prepared by a variety of synthetic methods. The common method is to react boric acid with the corresponding aromatic amine and cyclopropene methanesulfonic acid.
Safety Information:
- (4-(N-Cyclopropylsulfamoyl)-2-methylphenyl)boronic acid is relatively safe under correct handling and storage conditions. However, care should be taken to avoid direct contact with skin and eyes to avoid irritation.
-Wear appropriate personal protective equipment, such as lab gloves and safety glasses, to avoid inhaling dust or solution into the mouth or food.
-The handling and storage should follow the relevant safety procedures, and manage and dispose in accordance with local laws and regulations. Under improper use and disposal, may have adverse effects on the environment. Therefore, it is recommended to follow the correct laboratory safety operation guidelines.
Last Update：2024-04-09 20:45:29
