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376523 Sigma-Aldrich

3-(2-Bromoethyl)indole

97%

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Properties

Related Categories Building Blocks, C10, Chemical Synthesis, Halogenated Heterocycles, Heterocyclic Building Blocks,
assay   97%
mp   97-99 °C (lit.)
solubility   chloroform: soluble 25 mg/mL, clear, yellow
SMILES string   BrCCc1c[nH]c2ccccc12
InChI   1S/C10H10BrN/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2
InChI key   NTLAICDKHHQUGC-UHFFFAOYSA-N

Description

General description

3-(2-Bromoethyl)indole is a halogenated heterocyclic building block.

Application

3-(2-Bromoethyl)indole may be used in the synthesis of:
• β-carboline derivatives
• 6,7-dihydro-12H-indolo[2,3-a] pyridocolinium bromide
• N-(2-(3-indolyl)ethyl)aza-12-crown-4
• N-(2-(3-Indolyl)ethyl)aza-15-crown-5
• N-(2-(3-Indolyl)ethyl)aza-18-crown-6

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Meet Synthia - Retrosynthesis Sofware
Protocols & Articles

Articles

Indoles

Sigma-Aldrich is proud to offer a new series of ChemFiles—called Privileged Structures, to our Drug Discovery and Organic Synthesis customers. Each piece will highlight a specific motif, selected app...
Chemfiles Volume 4 Article 8
Keywords: Building blocks, Cardiovascular, Diabetes, Diseases, Drug discovery, Medicinal chemistry, Organic synthesis, Respiratory

Peer-Reviewed Papers
15

References

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