CAS 39891-70-8

Indoline-3-carboxylic acid

Description:

Indoline-3-carboxylic acid is an organic compound characterized by its indoline structure, which consists of a fused benzene and pyrrole ring, with a carboxylic acid functional group attached at the 3-position. This compound typically appears as a white to off-white solid and is known for its moderate solubility in polar solvents such as water and alcohols. Indoline-3-carboxylic acid exhibits properties typical of carboxylic acids, including the ability to form hydrogen bonds, which can influence its reactivity and interactions in various chemical environments. It is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its potential as a building block for more complex molecules. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, using appropriate safety measures to avoid exposure.

Formula: C₉H₉NO₂

InChI: InChI=1/C9H9NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-4,7,10H,5H2,(H,11,12)

SMILES: c1ccc2c(c1)C(CN2)C(=O)O

Synonyms:

• 1H-indole-3-carboxylic acid
• 2,3-Dihydro-
• 3-Indolinecarboxylic acid
• Acide 2,3-dihydro-1H-indole-3-carboxylique
• 2,3-dihydro-1H-indole-3-carboxylic acid
• INDOLINE-3-CARBOXYLIC ACID
• 1H-INDOLINE-3-CARBOXYLIC ACID

Indoline-3-carboxylic acid

CAS: 39891-70-8

Formula: C₉H₉NO₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 163.1733

Ref: IN-DA0076RY

Indoline-3-carboxylic acid

CAS: 39891-70-8

Indoline-3-carboxylic acid

Purity: 97%

Molecular weight: 163.17g/mol

Ref: 54-OR912928

1H-Indoline-3-carboxylic acid

CAS: 39891-70-8

1H-Indoline-3-carboxylic acid is a molecule with the chemical formula C8H6N2O2. It is an aromatic carboxylic acid and one of the three enantiopure isomers of indoline. 1H-Indoline-3-carboxylic acid has two tautomers, cis (cis) and trans (trans). The stereoisomer cis is found in nature, while trans can be synthesized. 1H-Indoline-3-carboxylic acid can be cleaved to form phenylacetic acid and benzoic acid in reactions catalyzed by acids at high temperatures. Kinetic studies have shown that 1H-indoline-3-carboxylic acid undergoes biotransformation to form methylbenzene, ethylbenzene, propylbenzene, butylbenzene, pentylbenzene and hexylbenzene.

Formula: C₉H₉NO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 163.17 g/mol

Ref: 3D-FI67496

Indoline-3-carboxylic acid

CAS: 39891-70-8

Formula: C₉H₉NO₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 163.176

Ref: 10-F209342