CAS 19012-03-4

1-Methylindole-3-carboxaldehyde

Description:

1-Methylindole-3-carboxaldehyde is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a methyl group at the nitrogen atom of the indole ring and an aldehyde functional group at the 3-position of the indole. It is typically a colorless to pale yellow liquid with a distinct aromatic odor. The presence of the aldehyde group makes it a reactive species, capable of participating in various chemical reactions, including condensation and oxidation. 1-Methylindole-3-carboxaldehyde is soluble in organic solvents and has limited solubility in water. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, due to its structural features, it may exhibit biological activity, making it of interest in medicinal chemistry and research. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₁₀H₉NO

InChI: InChI=1/C10H9NO/c1-11-6-8(7-12)9-4-2-3-5-10(9)11/h2-7H,1H3

InChI key: InChIKey=KXYBYRKRRGSZCX-UHFFFAOYSA-N

SMILES: C(=O)C=1C=2C(N(C)C1)=CC=CC2

Synonyms:

• 1-Methyl-1H-indole-3-carboxaldehyde
• 1-Methyl-3-formylindole
• 1-Methylindole-3-Carboxaldehyde
• 1-Methylindole-3-carbaldehyde
• 1H-Indole-3-carboxaldehyde, 1-methyl-
• 3-Formyl-1-methylindole
• Ai3-51477
• Indole-3-carboxaldehyde, 1-methyl-
• N-Methyl-3-formylindole
• N-Methyl-3-indolecarboxaldehyde
• N-Methylindole-3-carbaldehyde
• NSC 83042
• TIMTEC-BB SBB010057
• AKOS JY2082515
• 3-Formyl-1-methyl-1H-indole
• RARECHEM AH BS 0121
• ASINEX-REAG BAS 12967420
• 1-METHYL-1H-INDOLE-3-CARBALDEHYDE
• 1 METHYLINDOLE-3-ALDEHYDE
• 1-METHYLINDOLE-3-CARBOXALDEHYDE 98% (HPLC)
• 1-Methylindole-3-carboxaldehyde, 98+%

1-Methylindole-3-carboxaldehyde, 98+%

CAS: 19012-03-4

1-Methylindole-3-carboxaldehyde is used as a reactant for preparation of nitroolefins and -nitroalcohols via microwave- or ultrasound-assisted Henry reactions, reactant for synthesis of quinolinones via three-component Ugi reaction, reactant for synthesis of -ketoamides as inhibitors of Dengue virus

Formula: C₁₀H₉NO

Purity: 98+%

Color and Shape: Crystals or powder or crystalline powder, White to cream to pale brown or yellow

Molecular weight: 159.19

Ref: 02-L02212

1H-Indole-3-carboxaldehyde, 1-methyl-

CAS: 19012-03-4

Formula: C₁₀H₉NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 159.1846

Ref: IN-DA002EBZ

1-Methylindole-3-carboxaldehyde

CAS: 19012-03-4

Formula: C₁₀H₉NO

Molecular weight: 159.19

Ref: 7W-GK7378

1-Methyl-1H-indole-3-carboxaldehyde

CAS: 19012-03-4

1-Methyl-1H-indole-3-carboxaldehyde

Formula: C₁₀H₉NO

Purity: 98%

Color and Shape: light orange crystalline solid

Molecular weight: 159.18g/mol

Ref: 54-OR22346

1-Methyl-indole-3-carbaldehyde

CAS: 19012-03-4

Formula: C₁₀H₉NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 159.188

Ref: 10-F040213