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Catalog Number:
17214
CAS Number:
22190-33-6
5-Bromo-2,3-dihydro-1H-indole
Purity:
≥ 99% (GC)
Synonym(s):
5-Bromoindoline
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Product Information

5-Bromo-2,3-dihydro-1H-indole is a versatile chemical compound that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. This compound is recognized for its unique structure, which allows it to serve as a valuable intermediate in the synthesis of biologically active molecules. Researchers have utilized 5-Bromo-2,3-dihydro-1H-indole in the development of pharmaceuticals, particularly in the creation of novel indole derivatives that exhibit promising anti-cancer and anti-inflammatory properties. Its bromine substituent enhances reactivity, making it an ideal candidate for further functionalization, which can lead to the discovery of new therapeutic agents.

In addition to its pharmaceutical applications, 5-Bromo-2,3-dihydro-1H-indole is also employed in the field of materials science, where it can be used to synthesize advanced materials with specific electronic or optical properties. The compound's ability to undergo various chemical transformations allows for the design of materials tailored for specific applications, such as sensors or catalysts. With its broad range of applications and potential for innovation, 5-Bromo-2,3-dihydro-1H-indole is an essential compound for researchers and industry professionals looking to explore new frontiers in chemical synthesis and material development.

Synonyms
5-Bromoindoline
CAS Number
22190-33-6
Purity
≥ 99% (GC)
Molecular Formula
C8H8BrN
Molecular Weight
198.06
MDL Number
MFCD00027410
PubChem ID
3411566
Melting Point
36-43 ?C
Appearance
Pale cream to pink solid
Conditions
Store at ≤ -4 °C
General Information
Synonyms
5-Bromoindoline
CAS Number
22190-33-6
Purity
≥ 99% (GC)
Molecular Formula
C8H8BrN
Molecular Weight
198.06
MDL Number
MFCD00027410
PubChem ID
3411566
Melting Point
36-43 ?C
Appearance
Pale cream to pink solid
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Bromo-2,3-dihydro-1H-indole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in developing drugs targeting neurological disorders.
  • Organic Synthesis: It acts as a versatile building block in organic chemistry, allowing researchers to create complex molecules with specific functional groups, enhancing the efficiency of chemical synthesis.
  • Material Science: The compound is used in developing novel materials, including polymers and coatings, which can exhibit unique electrical and optical properties.
  • Biological Research: It is employed in studies investigating the mechanisms of action of certain biological pathways, providing insights into cellular processes and potential therapeutic targets.
  • Agrochemical Applications: This chemical can be utilized in the formulation of agrochemicals, contributing to the development of more effective pesticides and herbicides that are safer for the environment.

Citations