CAS 16382-15-3

Ethyl 5-methylindole-2-carboxylate

Description:

Ethyl 5-methylindole-2-carboxylate, with the CAS number 16382-15-3, is an organic compound that belongs to the class of indole derivatives. It features a carboxylate functional group and an ethyl ester, which contribute to its chemical reactivity and solubility properties. The structure includes a methyl group at the 5-position of the indole ring, which can influence its biological activity and interactions. This compound is typically characterized by its aromatic nature, which is indicative of the indole framework, and it may exhibit various chemical behaviors such as electrophilic substitution reactions due to the presence of the electron-rich indole system. Ethyl 5-methylindole-2-carboxylate is of interest in synthetic organic chemistry and may have applications in pharmaceuticals or agrochemicals, although specific biological activities or uses would depend on further research. Its physical properties, such as boiling point, melting point, and solubility, would need to be determined experimentally or sourced from reliable chemical databases for practical applications.

Formula: C₁₂H₁₃NO₂

InChI: InChI=1/C12H13NO2/c1-3-15-12(14)11-7-9-6-8(2)4-5-10(9)13-11/h4-7,13H,3H2,1-2H3

SMILES: CCOC(=O)c1cc2cc(C)ccc2[nH]1

Synonyms:

• 5-Methylindole-2-carboxylic acid ethyl ester
• ethyl 5-methyl-1H-indole-2-carboxylate
• ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
• 2-CARBOXY-5-METHYLINDOLE
• 5-Methyl-2-indolecarboxylic acid ethyl ester
• 5-Me-ICA-OEt
• 5-METHYL-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
• 2-CARBETHOXY-5-METHYLINDOLE

Ethyl 5-methylindole-2-carboxylate, 98%

CAS: 16382-15-3

Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions, reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists, reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents, reactant for Friedel-Craf

Formula: C₁₂H₁₃NO₂

Purity: 98%

Color and Shape: White or cream to pale brown, Powder

Molecular weight: 203.24

Ref: 02-L17146

1H-Indole-2-carboxylic acid, 5-methyl-, ethyl ester

CAS: 16382-15-3

Formula: C₁₂H₁₃NO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 203.2371

Ref: IN-DA001UFN

Ethyl 5-methylindole-2-carboxylate

CAS: 16382-15-3

Ethyl 5-methylindole-2-carboxylate

Formula: C₁₂H₁₃NO₂

Purity: 97%

Color and Shape: faint beige powder

Molecular weight: 203.24g/mol

Ref: 54-OR322120

Ethyl 5-methylindole-2-carboxylate

CAS: 16382-15-3

Ethyl 5-methylindole-2-carboxylate is an antioxidant that is used as a reagent in the synthesis of other compounds. It has been shown to inhibit cancer cell growth in vitro via its ability to inhibit the metabolic activity of human hepatoma cells. Ethyl 5-methylindole-2-carboxylate has also been shown to have cytotoxic activity against human hepatoma cells in vitro, and may be a potential anticancer drug candidate.

Formula: C₁₂H₁₃NO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 203.24 g/mol

Ref: 3D-FE56791

5-Methylindole-2-carboxylic acid ethyl ester

CAS: 16382-15-3

5-Methylindole-2-carboxylic acid ethyl ester is a fine chemical that belongs to the group of useful scaffold, versatile building block, and useful intermediate. It is used in research chemicals and speciality chemicals. 5-Methylindole-2-carboxylic acid ethyl ester is a complex compound with high quality and can be used as a reagent for producing other valuable compounds. 5-Methylindole-2-carboxylic acid ethyl ester also has the function of being a reaction component for producing other compounds.

Formula: C₁₂H₁₃NO₂

Molecular weight: 203.24 g/mol

Ref: 3D-M-4084

Ethyl 5-methylindole-2-carboxylate

CAS: 16382-15-3

Formula: C₁₂H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 203.241

Ref: 10-F222082