1704073-41-5

Basic information

• Product Name: (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid
• Synonyms: (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid
• CAS NO: 1704073-41-5
• Molecular Formula: C16H24BNO4
• Molecular Weight: 305.17706
• Mol File: 1704073-41-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 451.9±48.0 °C(Predicted)
• Appearance: /
• Density: 1.16±0.1 g/cm3(Predicted)
• PKA: 8?+-.0.16(Predicted)
• CAS DataBase Reference: (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid(1704073-41-5)
• EPA Substance Registry System: (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid(1704073-41-5)

Safety Data

• Hazardous Substances Data: 1704073-41-5(Hazardous Substances Data)

Usage

Description

(4-(1-((tert-butoxycarbonyl)(cyclopropyl)amino)ethyl)phenyl)boronic acid is a chemical compound with the molecular formula C17H24BNO4. It belongs to the class of boronic acids, which are widely used in organic synthesis and medicinal chemistry. (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid features a boronic acid group, a tert-butoxycarbonyl (Boc) protective group, and a cyclopropylamine group, which together contribute to its potential applications in the development of new drugs and as a chemical reagent in organic reactions.

Uses

Used in Medicinal Chemistry:
(4-(1-((tert-butoxycarbonyl)(cyclopropyl)amino)ethyl)phenyl)boronic acid is used as a building block for the synthesis of complex organic molecules and pharmaceuticals. The presence of the boronic acid group allows for versatile chemistry, enabling the formation of new carbon-carbon bonds and other functional groups, which can be crucial in the development of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (4-(1-((tert-butoxycarbonyl)(cyclopropyl)amino)ethyl)phenyl)boronic acid is used as a reagent for various chemical reactions. The Boc group serves as a protective group for the amine functionality, preventing unwanted side reactions and allowing for selective modification of other parts of the molecule. This selective protection can be advantageous in multi-step synthesis processes.
Used in Drug Development:
(4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid's structure, which includes a cyclopropylamine group, suggests potential biological activities that may be harnessed in drug development. The cyclopropylamine group can be a key component in the design of new drugs targeting specific receptors or enzymes, potentially leading to the discovery of new therapeutic agents for various diseases.
Used in Chemical Research:
(4-(1-((tert-butoxycarbonyl)(cyclopropyl)amino)ethyl)phenyl)boronic acid can be employed in academic and industrial research settings to study the reactivity and properties of boronic acids, as well as to explore new reaction mechanisms and synthetic strategies. (4-(1-((tert-butoxycarbonyl)(cyclopropyl)aMino)ethyl)phenyl)boronic acid can serve as a model system for understanding the fundamental principles of organic chemistry and potentially lead to new insights in the field.