884507-21-5

Basic information

• Product Name: 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine
• Synonyms: 1-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine;884507-21-5;1-[2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PYRROLIDINE;DTXSID401151444;AMY33029;CS-0045072;F15082;F76981;Pyrrolidine, 1-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
• CAS NO: 884507-21-5
• Molecular Formula: C16H24BNO2
• Molecular Weight: 273.2
• Mol File: 884507-21-5.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine(884507-21-5)
• EPA Substance Registry System: 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine(884507-21-5)

Safety Data

• Hazardous Substances Data: 884507-21-5(Hazardous Substances Data)

Usage

Description

1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is a chemical compound characterized by its molecular formula C17H27BO2N and a molecular weight of 297.21 g/mol. 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is distinguished by its unique reactivity and versatility in chemical reactions, stemming from the presence of a boron atom and a pyrrolidine group. The tetramethyl-substituted dioxaborolane moiety enhances the compound's stability and solubility, while the phenyl group contributes to its aromatic and electronic properties. As a result, 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is a valuable reagent in synthetic chemistry, particularly for the construction of complex organic molecules.

Uses

Used in Organic Synthesis:
1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is used as a reagent for the formation of carbon-carbon bonds in organic synthesis. Its unique reactivity, imparted by the boron atom, makes it a versatile compound for creating new carbon-carbon linkages, which are essential in the synthesis of a wide range of organic molecules.
Used in the Synthesis of Chiral Molecules:
The pyrrolidine group in 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine provides steric hindrance and chiral properties, making it an ideal reagent for the synthesis of chiral organic molecules. Chiral molecules are crucial in various applications, including pharmaceuticals, agrochemicals, and materials science, where enantioselectivity is a critical factor.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is used as a building block for the development of new drugs. Its ability to form carbon-carbon bonds and create chiral molecules makes it a valuable tool in the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Materials Science:
1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is also utilized in materials science for the synthesis of advanced materials with specific properties. 1-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine's ability to form carbon-carbon bonds and its aromatic and electronic properties make it suitable for the development of new materials with applications in various fields, such as electronics, energy storage, and polymer science.