913836-28-9

Basic information

• Product Name: 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE
• Synonyms: 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE;4-(PIPERIDINE-1-CARBONYLOXY)PHENYLBORONIC ACID, PINACOL ESTER;4-[(Piperidin-1-ylcarbonyl)oxy]benzeneboronic acid, pinacol ester;4-[(Piperidin-1-ylcarbonyl)oxy]benzeneboronic acid, pinacol ester 98%;4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl;4-(1-Piperidinylcarbonyloxy)benzeneboronic acid pinacol ester, 98%;4-[(Piperidin-1-ylcarbonyl)oxy]benzeneboronicacid,pinacolester98%
• CAS NO: 913836-28-9
• Molecular Formula: C18H26BNO4
• Molecular Weight: 331.22
• Product Categories: blocks;BoronicAcids
• Mol File: 913836-28-9.mol
• Article Data: 0

Chemical Properties

• Melting Point: 166-168℃
• Boiling Point: 443 °C at 760 mmHg
• Flash Point: 221.7 °C
• Appearance: /
• Density: 1.12 g/cm³
• Vapor Pressure: 4.79E-08mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE(913836-28-9)
• EPA Substance Registry System: 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE(913836-28-9)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 913836-28-9(Hazardous Substances Data)

Usage

Description

4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE is a complex organic compound that features a piperidine carboxylate group attached to a phenyl ring, which is further combined with a boron-containing 1,3,2-dioxaborolan-2-yl group. This unique structure positions it as a versatile molecule with potential applications in the fields of medicinal chemistry and organic synthesis.

Uses

Used in Medicinal Chemistry:
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE is used as a building block for the development of new pharmaceutical drugs. Its specific structure allows it to be a key component in the synthesis of various medicinal agents, potentially leading to the creation of novel therapeutics.
Used in Organic Synthesis:
In the realm of organic synthesis, 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE serves as a valuable reagent. Its ability to participate in a range of chemical reactions makes it useful for the synthesis of complex organic molecules, contributing to the advancement of chemical research and the discovery of new compounds.
Used in Pharmaceutical Drug Development:
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE is utilized in the pharmaceutical industry as a precursor in the synthesis of drug candidates. Its unique properties may contribute to the discovery of new drugs with improved efficacy and selectivity for various medical conditions.
Used in Organic Reactions:
As a reagent in organic reactions, 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE is employed to facilitate specific chemical transformations. Its presence can enhance the efficiency of certain synthetic pathways, making it an important tool for chemists in their quest to create new and useful organic compounds.
The specific applications and properties of 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL PIPERIDINE-1-CARBOXYLATE are subject to ongoing research and development, with its full potential yet to be fully realized in the scientific community.

InChI:InChI=1/C18H26BNO4/c1-17(2)18(3,4)24-19(23-17)14-8-10-15(11-9-14)22-16(21)20-12-6-5-7-13-20/h8-11H,5-7,12-13H2,1-4H3