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Catalog Number:
17139
CAS Number:
21109-25-1
1H-Indol-2-ylmethyl)amine
Purity:
≥ 95% (NMR)
Documents
$139.11 /250MG
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Product Information

(1H-Indol-2-ylmethyl)amine is a versatile compound recognized for its significant applications in pharmaceuticals and organic synthesis. This amine derivative of indole features a unique structure that allows it to act as a building block in the development of various bioactive molecules. Its ability to interact with biological systems makes it particularly valuable in medicinal chemistry, where it has been explored for potential therapeutic effects, including anti-cancer and anti-inflammatory properties. Researchers have utilized (1H-Indol-2-ylmethyl)amine in the synthesis of novel compounds that target specific biological pathways, showcasing its relevance in drug discovery and development.

In addition to its pharmaceutical applications, (1H-Indol-2-ylmethyl)amine serves as an important intermediate in the synthesis of agrochemicals and other fine chemicals. Its unique properties allow for the creation of compounds with enhanced efficacy and selectivity, making it a preferred choice among chemists in both academic and industrial settings. With its growing importance in various fields, (1H-Indol-2-ylmethyl)amine stands out as a compound with promising potential for innovation and development.

CAS Number
21109-25-1
Purity
≥ 95% (NMR)
Molecular Formula
C9H10N2
Molecular Weight
146.19
MDL Number
MFCD03422512
PubChem ID
582331
Appearance
Light brown solid
Conditions
Store at 0-8°C
General Information
CAS Number
21109-25-1
Purity
≥ 95% (NMR)
Molecular Formula
C9H10N2
Molecular Weight
146.19
MDL Number
MFCD03422512
PubChem ID
582331
Appearance
Light brown solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1H-Indol-2-ylmethyl)amine is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders due to its ability to interact with serotonin receptors.
  • Biological Research: It is employed in studies examining the role of indole derivatives in cell signaling and gene expression, providing insights into cellular mechanisms and potential therapeutic targets.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, that require specific chemical properties for enhanced performance.
  • Agrochemicals: It finds applications in the formulation of agrochemicals, contributing to the development of more effective and environmentally friendly pesticides and herbicides.
  • Diagnostic Tools: The compound is explored in the creation of diagnostic agents, particularly in imaging techniques that require specific binding properties to biological targets.

Citations