1449117-35-4

Basic information

• Product Name: 5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine
• Synonyms: 5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine;5-bromo-3-ethyl-2H-pyrazolo[3,4-b]pyridine
• CAS NO: 1449117-35-4
• Molecular Formula: C8H8BrN3
• Molecular Weight: 226.07322
• Mol File: 1449117-35-4.mol

Chemical Properties

• Boiling Point: 345.3±37.0 °C(Predicted)
• Appearance: /
• Density: 1.646±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 9.05±0.40(Predicted)
• CAS DataBase Reference: 5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine(1449117-35-4)
• EPA Substance Registry System: 5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine(1449117-35-4)

Safety Data

• Hazardous Substances Data: 1449117-35-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Drug Development:
5-Bromo-3-ethyl-1H-pyrazolo[3,4-b]pyridine is used as a research compound for its ability to bind to specific receptors in the central nervous system. Its interaction with these receptors can provide insights into the development of new therapeutics targeting neurological disorders and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 5-Bromo-3-ethyl-1H-pyrazolo[3,4-b]pyridine serves as a building block for the construction of more complex molecules. Its unique structure allows for the creation of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in the Study of Molecular Interactions:
5-broMo-3-ethyl-1H-pyrazolo[3,4-b]pyridine's unique structure and properties make it a valuable tool for studying the interactions between small molecules and biological targets. This can lead to a better understanding of molecular recognition processes and the development of more effective drugs with fewer side effects.
Used in the Development of New Therapeutics:
5-Bromo-3-ethyl-1H-pyrazolo[3,4-b]pyridine has potential applications in the development of new therapeutics due to its ability to modulate specific biological pathways. Its unique chemical properties can be leveraged to design drugs with improved efficacy and selectivity, ultimately benefiting patients with various diseases and conditions.