1557780-95-6

Basic information

• Product Name: 1-Boc-6-chloro-3-iodo-1H-indole
• Synonyms: 1-Boc-6-chloro-3-iodo-1H-indole
• CAS NO: 1557780-95-6
• Molecular Formula: C13H13ClINO2
• Molecular Weight: 377.60529
• Mol File: 1557780-95-6.mol

Chemical Properties

• Boiling Point: 417.1±48.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-Boc-6-chloro-3-iodo-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Boc-6-chloro-3-iodo-1H-indole(1557780-95-6)
• EPA Substance Registry System: 1-Boc-6-chloro-3-iodo-1H-indole(1557780-95-6)

Safety Data

• Hazardous Substances Data: 1557780-95-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-Boc-6-chloro-3-iodo-1H-indole serves as a key synthetic intermediate for the creation of various heterocyclic compounds, which are often found in pharmaceuticals. Its presence of a chloro and iodo group on the indole ring allows for further functionalization and modification, making it a versatile building block for the synthesis of potential drug candidates.
Used in Organic Synthesis:
As a synthetic intermediate, 1-Boc-6-chloro-3-iodo-1H-indole is utilized in organic synthesis to construct complex organic molecules. The Boc protecting group on the nitrogen atom ensures that the amine remains protected during the synthesis process, facilitating the formation of desired products without unwanted side reactions.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-Boc-6-chloro-3-iodo-1H-indole is employed for the development of new therapeutic agents. Its structural features, including the Boc protecting group and the halogenated indole ring, make it a valuable precursor for the synthesis of bioactive molecules with potential applications in treating various diseases and medical conditions.
Used as a Molecular Probe in Biological Studies:
1-Boc-6-chloro-3-iodo-1H-indole also has potential applications as a molecular probe in biological research. Its unique chemical properties and reactivity can be exploited to investigate biological processes, interactions, and mechanisms, contributing to a deeper understanding of biological systems and the discovery of novel therapeutic targets.