1256359-13-3

Basic information

• Product Name: 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4-Isopropylsulfonylphenylboronic acid, pinacol ester
• CAS NO: 1256359-13-3
• Molecular Formula: C₁₅H₂₃BO₄S
• Molecular Weight: 310.21672
• Mol File: 1256359-13-3.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 439.4±37.0 °C(Predicted)
• Appearance: /
• Density: 1.13±0.1 g/cm3(Predicted)
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1256359-13-3)
• EPA Substance Registry System: 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1256359-13-3)

Safety Data

• Hazardous Substances Data: 1256359-13-3(Hazardous Substances Data)

Usage

General Description

2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound that has a boron atom and is widely used as a reagent in organic synthesis. It is commonly used in the Suzuki coupling reaction, which is a valuable tool for creating carbon-carbon bonds. 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is known for its high stability, low toxicity, and suitability for use in a wide range of reactions. Its unique structure and reactivity make it a valuable tool in the field of medicinal chemistry and materials science, where it is used for creating complex organic molecules and functional materials.

Downstream Products

• 1349151-91-2 5-(4-isopropylsulfonylphenyl)-3-(2-phenylethynyl)pyrazin-2-amine 
• 1232424-98-4 3-amino-6-(4-(isopropylsulfonyl)phenyl)pyrazine-2-carboxylic acid 
• 1349770-61-1 tert-butyl N-[[4-[5-[2-[bis(tert-butoxycarbonyl)amino]-5-(4-isopropylsulfonylphenyl)-3-pyridyl]-1,3,4-oxadiazol-2-yl]phenyl]methyl]-N-methyl-carbamate