CAS 5585-96-6

4-indolyl acetate

Description:

4-Indolyl acetate, with the CAS number 5585-96-6, is an organic compound that belongs to the class of indole derivatives. It features an indole ring structure, which is a bicyclic compound consisting of a fused benzene and pyrrole ring, with an acetate group attached at the 4-position of the indole. This compound is typically a white to off-white solid and is known for its moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water. 4-Indolyl acetate is of interest in various fields, including medicinal chemistry and biochemistry, due to its potential biological activities, including anti-inflammatory and anticancer properties. It can also serve as a precursor in the synthesis of other indole derivatives. As with many organic compounds, handling should be done with care, observing appropriate safety protocols to mitigate any risks associated with its use.

Formula: C₁₀H₉NO₂

InChI: InChI=1/C10H9NO2/c1-7(12)13-10-4-2-3-9-8(10)5-6-11-9/h2-6,11H,1H3

SMILES: CC(=O)Oc1cccc2c1cc[nH]2

Synonyms:

• 4-Indoxyl acetate
• 1H-indol-4-yl acetate
• 4-Acetoxyindole

1H-Indol-4-yl acetate

CAS: 5585-96-6

Formula: C₁₀H₉NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 175.1840

Ref: IN-DA003LK2

1H-Indol-4-yl acetate

CAS: 5585-96-6

Formula: C₁₀H₉NO₂

Purity: 98.0%

Color and Shape: Solid, Powder or Crystalline Powder or Solid

Molecular weight: 175.187

Ref: 10-F226279

4-Acetoxyindole

CAS: 5585-96-6

4-Acetoxyindole

Formula: C₁₀H₉NO₂

Purity: 98%

Color and Shape: light beige solid

Molecular weight: 175.18g/mol

Ref: 54-OR2401

4-Acetoxyindole

CAS: 5585-96-6

4-Acetoxyindole is a chromophore that belongs to the pyrrole family of compounds. It has been shown to react with an ionic liquid under acidic conditions to form a protonated intermediate, which can be deprotonated by a nucleophile. This reaction yields an acetate anion and a fluorescing product. 4-Acetoxyindole also reacts with deuterium gas, yielding an acetate, a deuterium atom, and fluorescing product. The reaction is reversible and the yield of the product depends on the concentration of the reactants. 4-Acetoxyindole has strong carbonyl groups that make it reactive towards other functional groups. These reactions are useful for synthesizing heterocycles such as indoles and isoquinolines.

Formula: C₁₀H₉NO₂

Purity: Min. 97 Area-%

Color and Shape: White Powder

Molecular weight: 175.18 g/mol

Ref: 3D-FA03468

4-Acetoxyindole

Controlled Product

CAS: 5585-96-6

Applications 4-Acetoxyindole is a useful intermediate for organic synthesis of Psilocine and Psilocine analogs.
References Julia, M., et al.: Chimica Therapeutica, 5, 279 (1970); Repke, D. B., et al.: J. Heterocycl. Chem., 14, 71 (1977)

Formula: C₁₀H₉NO₂

Color and Shape: Neat

Molecular weight: 175.18

Ref: TR-A165853

4-Acetoxyindole

CAS: 5585-96-6

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Formula: C₁₀H₉NO₂

Purity: Min. 98.0 Area-%

Molecular weight: 175.19 g/mol

Ref: 3D-A-0300