957120-95-5

Basic information

• Product Name: 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid
• Synonyms: 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid
• CAS NO: 957120-95-5
• Molecular Formula: C16H14BNO4S
• Molecular Weight: 327.17
• Product Categories: blocks;BoronicAcids;Sulfonamides
• Mol File: 957120-95-5.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid(957120-95-5)
• EPA Substance Registry System: 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid(957120-95-5)

Safety Data

• Hazardous Substances Data: 957120-95-5(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid is used as a reagent in organic synthesis for forming carbon-carbon bonds through the Suzuki-Miyaura coupling reactions, which is crucial for the creation of complex organic molecules and pharmaceutical compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid is used as a therapeutic agent for its potential in treating cancer. It targets specific proteins and enzymes involved in cancer development and progression, offering a promising avenue for cancer treatment.
Used in Inflammatory Disease Treatment:
4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid also serves as a therapeutic agent in the treatment of inflammatory diseases, leveraging its ability to modulate proteins and enzymes that contribute to inflammation, thereby providing potential relief and management of these conditions.
Used in Chemical and Biological Research:
Due to its solubility and stability provided by the sulfamoyl group, 4-(N-Naphthalen-1-ylsulfamoyl)phenylboronic acid is used as a versatile tool in chemical and biological research, facilitating the study of molecular interactions and the development of new drugs and materials.