CAS 942-24-5

Methyl indole-3-carboxylate

Description:

Methyl indole-3-carboxylate, with the CAS number 942-24-5, is an organic compound that belongs to the class of indole derivatives. It features a methyl ester functional group attached to the indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound is typically characterized by its aromatic properties, contributing to its stability and reactivity. Methyl indole-3-carboxylate is often used in organic synthesis and medicinal chemistry due to its potential biological activities, including anti-inflammatory and anticancer properties. It is generally soluble in organic solvents such as ethanol and dichloromethane, while being less soluble in water. The compound can undergo various chemical reactions, including esterification and hydrolysis, making it a versatile intermediate in the synthesis of more complex molecules. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₀H₉NO₂

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

SMILES: COC(=O)c1c[nH]c2ccccc12

Synonyms:

• 1H-Indole-3-carboxylic acid, methyl ester
• Indole-3-carboxylic acid, methyl ester
• methyl 1H-indole-3-carboxylate
• METHYL-(3-INDOLCARBOXYLATE)
• RARECHEM AH BS 0112
• Methylindole-3-Carboxylate99%
• methyl indoline-3-carboxylate
• METHYL INDOLE-3-CARBOXYLATE
• 3-Indolecarboxylic acid methyl ester

Methyl Indole-3-carboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Purity: >98.0%(GC)

Color and Shape: White to Gray to Brown powder to crystal

Molecular weight: 175.19

Ref: 3B-I0491

Methyl indole-3-carboxylate, 99%

CAS: 942-24-5

Reactant used for preparation of nitric oxide synthesis (nNOS) inhibitors, protein kinase c alpha (PKC) inhibitors, inhibitors of the C-terminal domain of RNA polymerase II as antitumor agents, kinase insert domain receptor (KDR) inhibitors, organocatalysts for the anti-Mannich reaction, very late a

Formula: C₁₀H₉NO₂

Purity: 99%

Color and Shape: Powder or lumps, White to cream to dark cream to brown or purple to dark pink to pale pink

Molecular weight: 175.19

Ref: 02-L14516

methyl indole-3-carboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Purity: 95.99%

Color and Shape: Brownish. Solid

Molecular weight: 175.0

Ref: 8R-CL0458

Methyl indole-3-carboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 175.1840

Ref: IN-DA003RKD

Methyl indole-3-carboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Molecular weight: 175.19

Ref: 7W-GK8552

Methyl indole-3-carboxylate

CAS: 942-24-5

Methyl indole-3-carboxylate

Formula: C₁₀H₉NO₂

Purity: 98%

Color and Shape: pale yellow solid

Molecular weight: 175.18g/mol

Ref: 54-OR5733

Methyl indole-3-carboxylate

CAS: 942-24-5

Methyl indole-3-carboxylate

Purity: ≥98%

Molecular weight: 175.18g/mol

Ref: 54-BUP19070

Methyl 3-indolecarboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 175.187

Ref: BP-SBP00701

Methyl indole-3-carboxylate

CAS: 942-24-5

Methyl indole-3-carboxylate (Methyl 3-indolecarboxylate) is a natural product isolated from Heracleum candicans.

Formula: C₁₀H₉NO₂

Purity: 99.41%

Color and Shape: Light Pink Powder

Molecular weight: 175.18

Ref: TM-T5868

Methyl indole-3-carboxylate

Controlled Product

CAS: 942-24-5

Applications Methyl indole-3-carboxylate is a reagent in the preaparation of oncrasin-1 derivatives which is a novel inhibitor of the C-terminal domain of RNA polymerase II.
References Wu, S., et al.: J. Med. Chem., 54, 2668 (2011);

Formula: C₁₀H₉NO₂

Color and Shape: Neat

Molecular weight: 175.18

Ref: TR-M313520

Indole-3-carboxylic acid methyl ester

Controlled Product

CAS: 942-24-5

Indole-3-carboxylic acid methyl ester is a quinoline derivative that is structurally related to the well-known antibiotic, ciprofloxacin. It has been shown to be cytotoxic against a variety of bacterial strains including Pseudomonas aeruginosa and Staphylococcus aureus. The mechanism of action for this compound is not yet fully understood, but it has been shown to inhibit collagen production in cell cultures and induce neuronal death in mice. Indole-3-carboxylic acid methyl ester also possesses anti-cancer properties and inhibits fatty acid synthesis. This compound also has antifungal effects against Candida albicans and other fungi.

Formula: C₁₀H₉NO₂

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 175.18 g/mol

Ref: 3D-FI30467

Methyl indole-3-carboxylate

CAS: 942-24-5

Formula: C₁₀H₉NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 175.187

Ref: 10-F003455