CAS 22948-94-3

N-Acetylindole-3-carboxaldehyde

Description:

N-Acetylindole-3-carboxaldehyde, with the CAS number 22948-94-3, is an organic compound that features a fused indole structure with an acetyl group and an aldehyde functional group. This compound typically appears as a yellow to brown solid or crystalline substance. It is characterized by its aromatic properties due to the indole moiety, which contributes to its potential biological activity. The presence of the aldehyde group makes it reactive, allowing for various chemical transformations, including condensation reactions. N-Acetylindole-3-carboxaldehyde is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its solubility can vary depending on the solvent, but it is generally soluble in organic solvents like ethanol and dichloromethane. Additionally, this compound may exhibit fluorescence, making it useful in certain analytical applications. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity and reactivity.

Formula: C₁₁H₉NO₂

InChI: InChI=1S/C11H9NO2/c1-8(14)12-6-9(7-13)10-4-2-3-5-11(10)12/h2-7H,1H3

InChI key: InChIKey=LCJLFGSKHBDOAY-UHFFFAOYSA-N

SMILES: C(C)(=O)N1C=2C(C(C=O)=C1)=CC=CC2

Synonyms:

• 1-Acetyl-1H-indole-3-carbaldehyde
• 1-Acetyl-1H-indole-3-carboxaldehyde
• 1-Acetyl-3-formyl-1H-indole
• 1-Acetyl-3-formylindole
• 1-Acetylindole-3-carbaldehyde
• 1-Acetylindole-3-carboxaldehyde
• 1H-Indole-3-carboxaldehyde, 1-acetyl-
• Indole-3-carboxaldehyde, 1-acetyl-
• N-Acetyl-1H-indole-3-carboxaldehyde
• N-Acetyl-3-indolecarboxaldehyde
• N-Acetylindol-3-carboxaldehyde
• NSC 61289

1H-Indole-3-carboxaldehyde, 1-acetyl-

CAS: 22948-94-3

Formula: C₁₁H₉NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 187.1947

Ref: IN-DA002LMN

1-Acetyl-1H-indole-3-carboxaldehyde

CAS: 22948-94-3

1-Acetyl-1H-indole-3-carboxaldehyde

Formula: C₁₁H₉NO₂

Purity: ≥95%

Color and Shape: faint orange crystalline powder

Molecular weight: 187.19466g/mol

Ref: 54-OR6847

1-Acetylindole-3-carboxaldehyde

CAS: 22948-94-3

1-Acetylindole-3-carboxaldehyde is a versatile building block that can be used as a reagent and reaction component in many organic syntheses. It is an important intermediate for the synthesis of various heterocycles, such as indoles, benzofurans, benzothiophenes and indazoles. 1-Acetylindole-3-carboxaldehyde is also a useful building block for the synthesis of complex compounds with a wide range of applications. This compound has been used in the preparation of a number of pharmaceuticals, including antidiabetic drugs, antihistamines and antipsychotics. It can also be used to make fine chemicals such as herbicides and insecticides.

Formula: C₁₁H₉NO₂

Purity: Min. 99 Area-%

Molecular weight: 187.20 g/mol

Ref: 3D-A-1400

1-Acetyl-1H-indole-3-carbaldehyde

CAS: 22948-94-3

Formula: C₁₁H₉NO₂

Purity: 97%

Color and Shape: Solid, Crystalline

Molecular weight: 187.198

Ref: 10-F210007

1-Acetyl-3-indolecarboxaldehyde

CAS: 22948-94-3

1-Acetyl-3-indolecarboxaldehyde is a ligand that binds to the cannabinoid receptor 1 (CB1). It has been shown to bind to the CB1 receptor with high affinity and selectivity. In addition, it has been demonstrated to inhibit the proliferation of human breast cancer cells in vitro. The compound is used as a fluorescent probe for cb1 receptor binding. Data obtained from molecular modelling studies have suggested that the hydroxyl group might be involved in binding to the CB1 receptor. 1-Acetyl-3-indolecarboxaldehyde also binds carotenoids, which are molecules responsible for giving plants and other photosynthetic organisms their coloration. This compound can be found in many different plants, such as carrots and bananas, where it acts as an antioxidant.

Formula: C₁₁H₉NO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 187.19 g/mol

Ref: 3D-FA30363