(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid
CAS: 1217501-46-6
Molecular Formula: C9H14BNO4S
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid - Names and Identifiers
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid - Physico-chemical Properties
| Molecular Formula | C9H14BNO4S |
| Molar Mass | 243.09 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD13195667 |
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid - Introduction
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid, also known as (4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid, is an organic boron compound. The following is a description of its nature, use, preparation and safety information:
Nature:
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid is a white solid with thermal stability and solubility. Its chemical structure contains amino and alkyl substituents.
Use:
The compound is widely used in the field of organic synthesis, especially as a ligand in metal complex catalytic reactions. It can be used in the synthesis of organic compounds such as aromatic aldehydes, ketones, amines, etc. In addition,(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid can also be used in biomedical research, such as for the preparation of pharmaceutical intermediates.
Preparation Method:
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid is generally prepared by organic chemical synthesis. It can be reacted with benzaldehyde and p-toluene boronic acid, followed by reaction with ethylsulfamoyl chloride to give the final product.
Safety Information:
For specific safety information on (4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid, it is recommended to refer to the relevant safety data form (SDS) provided by the chemical supplier. Appropriate laboratory practices and personal protective measures should be taken when handling the compound to avoid contact with skin, eyes, and respiratory tract.
Nature:
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid is a white solid with thermal stability and solubility. Its chemical structure contains amino and alkyl substituents.
Use:
The compound is widely used in the field of organic synthesis, especially as a ligand in metal complex catalytic reactions. It can be used in the synthesis of organic compounds such as aromatic aldehydes, ketones, amines, etc. In addition,(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid can also be used in biomedical research, such as for the preparation of pharmaceutical intermediates.
Preparation Method:
(4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid is generally prepared by organic chemical synthesis. It can be reacted with benzaldehyde and p-toluene boronic acid, followed by reaction with ethylsulfamoyl chloride to give the final product.
Safety Information:
For specific safety information on (4-(N-Ethylsulfamoyl)-2-methylphenyl)boronic acid, it is recommended to refer to the relevant safety data form (SDS) provided by the chemical supplier. Appropriate laboratory practices and personal protective measures should be taken when handling the compound to avoid contact with skin, eyes, and respiratory tract.
Last Update：2024-04-09 15:18:10
