CAS 59040-84-5

Methyl indoline-2-carboxylate

Description:

Methyl indoline-2-carboxylate is an organic compound characterized by its indoline structure, which features a fused bicyclic system comprising a benzene ring and a pyrrole-like ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It possesses a carboxylate functional group, which contributes to its reactivity and solubility in various solvents. Methyl indoline-2-carboxylate is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to undergo various chemical transformations. The compound may exhibit biological activity, making it of interest in medicinal chemistry. Its molecular structure allows for interactions with biological targets, which can be explored in drug discovery. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken. Overall, methyl indoline-2-carboxylate is a versatile compound with significant implications in chemical research and industry.

Formula: C₁₀H₁₁NO₂

InChI: InChI=1S/C10H11NO2/c1-13-10(12)9-6-7-4-2-3-5-8(7)11-9/h2-5,9,11H,6H2,1H3

InChI key: InChIKey=URORFKDEPJFPOV-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1CC=2C(N1)=CC=CC2

Synonyms:

• Indoline-2-carboxylic acid methyl ester
• 1H-Indole-2-carboxylic acid, 2,3-dihydro-, methyl ester
• 2-Methoxycarbonylindoline
• 2,3-Dihydroindole-2-carboxylic acid methyl ester
• Methyl indoline-2-carboxylate

2,3-Dihydro-1H-indole-2-carboxylic acid methyl ester

CAS: 59040-84-5

2,3-Dihydro-1H-indole-2-carboxylic acid methyl ester

Purity: 95%

Molecular weight: 177.20g/mol

Ref: 54-OR955713

Methyl indoline-2-carboxylate

CAS: 59040-84-5

Purity: 98%

Molecular weight: 177.2030029

Ref: 10-F620224

methyl 2,3-dihydro-1H-indole-2-carboxylate

CAS: 59040-84-5

Methyl 2,3-dihydro-1H-indole-2-carboxylate is an optical isomer of 1,3,5-trimethyl indole. It is a reactive compound that can undergo transesterification reaction with methyl esters or nitroindoles to form antibiotics. Methyl 2,3-dihydro-1H-indole-2-carboxylate has been shown to inhibit the activity of cyclooxygenase and lipase enzymes by forming allyl carbonates. The chemical parameters of this compound have been studied using nuclear magnetic resonance spectroscopy (NMR) and kinetic methods.

Formula: C₁₀H₁₁NO₂

Purity: Min. 95%

Molecular weight: 177.2 g/mol

Ref: 3D-JCA04084