4-Bromoindole, 98%
4-Bromoindole, 98%
4-Bromoindole, 98%
Thermo Scientific Chemicals

4-Bromoindole, 98%

CAS: 52488-36-5 | C8H6BrN | 196.047 g/mol
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1 g
5 g
Catalog number L19417.06
also known as L19417-06
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202,00
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Quantity:
5 g
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Price (EUR)
202,00
Each
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Chemical Identifiers
CAS52488-36-5
IUPAC Name4-bromo-1H-indole
Molecular FormulaC8H6BrN
InChI KeyGRJZJFUBQYULKL-UHFFFAOYSA-N
SMILESBrC1=C2C=CNC2=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Yellow to dark brown or very dark red/brown
FormLiquid
Assay (GC)≥95.0%
Refractive Index1.6520-1.6610 @20°C
4-Bromoindole is a potential inhibitor of GSK-3. It is also used as pharmaceutical intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Bromoindole is a potential inhibitor of GSK-3. It is also used as pharmaceutical intermediates.

Solubility
Not miscible in water.

Notes
Air & Light Sensitive. Store at 4°C. Store in the dark. Store under dry inert gas. Protect from heat. Incompatible with heat. light, air.
RUO – Research Use Only

General References:

  1. Yuusaku Yokoyama; Hidemasa Hikawa; Masaharu Mitsuhashi; Aki Uyama; Yasuoki Murakami. Syntheses without protection: a three-step synthesis of optically active clavicipitic acid by utilizing biomimetic synthesis of 4-bromotryptophan. Tetrahedron Letters.1999, 40, 7803-7806.
  2. Mark C Bagley; Christopher J Moody; Adrian G Pepper. Studies towards the synthesis of diazonamide A. Synthesis of the 4-(oxazol-5-ylmethyl) aryltryptamine fragment. Tetrahedron Letters.2000, 41, 6901-6904.