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Catalog Number:
44516
CAS Number:
32774-29-1
5-Bromoindole-3-éthanol
Purity:
≥ 98% (CG)
Synonym(s):
5-Bromo-3-(2-hydroxyéthyl)indole
Documents
$136.91 /250 mg
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Product Information

5-Bromoindole-3-ethanol is a versatile compound recognized for its significant role in pharmaceutical and biochemical research. This compound, characterized by its bromine substitution on the indole ring, exhibits unique properties that make it valuable in the synthesis of various bioactive molecules. Researchers utilize 5-Bromoindole-3-ethanol in the development of novel pharmaceuticals, particularly in the exploration of anti-cancer and anti-inflammatory agents. Its ability to act as a building block in organic synthesis allows for the creation of complex structures, enhancing its relevance in medicinal chemistry.

In addition to its applications in drug discovery, 5-Bromoindole-3-ethanol serves as a useful tool in biochemical assays and studies involving serotonin receptors, making it an essential compound for neuropharmacology research. Its unique structure and reactivity provide researchers with a reliable option for exploring new therapeutic avenues. With its proven efficacy and adaptability, 5-Bromoindole-3-ethanol stands out as a key compound for professionals seeking innovative solutions in chemical synthesis and biological research.

Synonyms
5-Bromo-3-(2-hydroxyéthyl)indole
CAS Number
32774-29-1
Purity
≥ 98% (CG)
Molecular Formula
C10H10BrNO
Molecular Weight
240.1
MDL Number
MFCD00130167
PubChem ID
122956
Melting Point
83 - 87 °C
Appearance
Poudre blanche à orange à verte à cristal
Conditions
Magasin chez RT
General Information
Synonyms
5-Bromo-3-(2-hydroxyéthyl)indole
CAS Number
32774-29-1
Purity
≥ 98% (CG)
Molecular Formula
C10H10BrNO
Molecular Weight
240.1
MDL Number
MFCD00130167
PubChem ID
122956
Melting Point
83 - 87 °C
Appearance
Poudre blanche à orange à verte à cristal
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromoindole-3-ethanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Biochemical Research: It is employed in studies investigating serotonin receptors, contributing to our understanding of mood regulation and potential treatments for depression.
  • Material Science: The compound is used to create advanced materials with unique electronic properties, which can be beneficial in the development of organic semiconductors.
  • Fluorescent Probes: 5-Bromoindole-3-ethanol is utilized in the design of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Agrochemical Applications: It has potential uses in the formulation of agrochemicals, enhancing crop protection products through its biological activity against pests.

Citations