1704069-47-5

Basic information

• Product Name: (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid
• Synonyms: (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid
• CAS NO: 1704069-47-5
• Molecular Formula: C17H27BN2O4
• Molecular Weight: 334.21828
• Mol File: 1704069-47-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 465.5±55.0 °C(Predicted)
• Appearance: /
• Density: 1.17±0.1 g/cm3(Predicted)
• PKA: 8.67±0.17(Predicted)
• CAS DataBase Reference: (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid(1704069-47-5)
• EPA Substance Registry System: (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid(1704069-47-5)

Safety Data

• Hazardous Substances Data: 1704069-47-5(Hazardous Substances Data)

Usage

Description

(4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid is a boronic acid derivative that features a phenyl group and a piperazine moiety. (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid is utilized in organic synthesis and medicinal chemistry as a key building block for the creation of a variety of pharmaceutical compounds. The presence of a tert-butoxycarbonyl (Boc) group on the nitrogen of the piperazine serves a protective role, allowing for selective chemical reactions to occur. The boronic acid group endows this molecule with the capacity for cross-coupling reactions with other organic molecules, rendering it a highly versatile reagent in the field of synthetic chemistry. Furthermore, the piperazine component can engage with biological targets, which positions this compound as a valuable asset in drug design and development.

Uses

Used in Organic Synthesis:
(4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid is used as a building block for the synthesis of pharmaceutical compounds due to its ability to participate in cross-coupling reactions with other organic molecules, facilitating the creation of a diverse range of chemical entities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid is used as a versatile reagent for the development of new drugs. Its protective Boc group allows for selective reactions, while the piperazine moiety can interact with biological targets, making it instrumental in the design and synthesis of potential therapeutic agents.
Used in Drug Design and Development:
(4-(1-(4-(tert-butoxycarbonyl)piperazin-1-yl)ethyl)phenyl)boronic acid is utilized as a component in drug design and development because of its potential to engage with biological targets. This interaction capability, combined with its synthetic versatility, makes it a promising candidate for the creation of new pharmaceuticals with specific therapeutic effects.