CAS 96056-64-3
:(S)-(-)-Indoline-2-carboxylic acid
Description:
(S)-(-)-Indoline-2-carboxylic acid is an organic compound characterized by its indoline structure, which consists of a fused benzene and pyrrole ring. This compound features a carboxylic acid functional group (-COOH) at the 2-position of the indoline ring, contributing to its acidic properties. It is a chiral molecule, with the (S)-(-) designation indicating its specific stereochemistry, which can influence its biological activity and interactions. The compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, while being less soluble in non-polar solvents. Its applications may include use in pharmaceuticals, particularly in the synthesis of biologically active compounds, and as a potential building block in organic synthesis. The presence of the carboxylic acid group allows for various chemical reactions, including esterification and amidation, making it versatile in synthetic chemistry. As with many organic acids, it may exhibit moderate toxicity and should be handled with appropriate safety precautions.
Formula:C9H9NO2
InChI:InChI=1/C9H9NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-4,8,10H,5H2,(H,11,12)/t8-/m1/s1
SMILES:c1ccc2c(c1)C[C@H](C(=O)O)N2
Synonyms:- Perindopril Intermediate
- (2S)-indoline-2-carboxylic acid
- (2S)-2,3-dihydro-1H-Indole-2-carboxylic acid
- (S)-(-)-Indoline-2-CarboxylicAcid
- S-(-)-Oindolium-2-CarboxylicAcid
- methyl 2,3-dihydro-1H-indole-2-carboxylate
- S-(-)-Indoline-2-carboxylic acid
- S-Indoline-2-carboxylic acid
- (S)-indoline-2-carboxylic acid
- (S)-(-)-Indoline-2-carboxylic acid
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Found 4 products.
(S)-Methyl indoline-2-carboxylate hydrochloride
CAS:Formula:C10H12ClNO2Purity:98%Color and Shape:SolidMolecular weight:213.6608(S)-Methyl indoline-2-carboxylate hydrochloride
CAS:(S)-Methyl indoline-2-carboxylate hydrochloridePurity:98%Molecular weight:213.66g/molmethyl (S)-indoline-2-carboxylate hydrochloride
CAS:<p>Methyl (S)-indoline-2-carboxylate hydrochloride is a lipase inhibitor that belongs to the class of antibiotics. It inhibits the lipid acylase by reversibly binding to the enzyme and blocking the esterification reaction. The interaction between methyl (S)-indoline-2-carboxylate hydrochloride and the enzyme is reversible, which allows for a kinetic analysis of the inhibition. Methyl (S)-indoline-2-carboxylate hydrochloride has been shown to inhibit cyclic nitroindole synthesis in vitro, but not in vivo. This compound also interacts with o-glycosylations, as it can be seen with its optical rotation. Methyl (S)-indoline-2-carboxylate hydrochloride has been shown to have an effect on allyl carbonates, which have similar ring structures as glycosides.</p>Formula:C10H12ClNO2Purity:Min. 95%Molecular weight:213.66 g/mol



