L-Indoline-2-carboxylic acid

CAS: 79815-20-6

Ref. 3D-FI56032

Produktinformation

• Name: L-Indoline-2-carboxylic acid
• Synonyme: (S)-(-)-Indoline-2-carboxylic acid(S)-2,3-Dihydro-1H-indole-2-carboxylic acid, (-)-(S)-2-Indolinecarboxylic acid, (-)-2,3-Dihydroindole-2-carboxylic acid, (2S)-2,3-Dihydroindole-2-carboxylic acid, (2S)-2,3-dihydro-1H-Indole-2-carboxylic acid, (2S)-2-Indolinecarboxylic acid, (2S)-indoline-2-carboxylic acid, (S)-(-)-Indoline-2-CarboxylicAcid, (S)-2,3-Dihydro-1H-indole-2-carboxylic acid, (S)-2-Carboxyindoline, 1H-Indole-2-carboxylic acid, 2,3-dihydro-, (2S)-, 1H-Indole-2-carboxylic acid, 2,3-dihydro-, (S)-, <span class="text-smallcaps">L</span>-Indoline-2-carboxylic acid, Perindopril Intermediate, S-(-)-Oindolium-2-CarboxylicAcid, methyl 2,3-dihydro-1H-indole-2-carboxylate
• CAS: 79815-20-6

Beschreibung

L-Indoline-2-carboxylic acid is a chiral organic compound that can be used as an asymmetric synthesis substrate. It is a nitro compound that has been shown to inhibit the growth of bacteria in the environment, such as Pseudomonas aeruginosa and Escherichia coli. L-Indoline-2-carboxylic acid is found to have a stereoselective nitro group at position 3, which means it can be used for the production of l-phenylalanine from nitrobenzene. It also has conformational properties and can be immobilized on an agarose gel. This chemical may be involved in ganglion cell death due to its ability to induce deformation of these cells in culture. L-Indoline-2-carboxylic acid also has enzymatic activity when it acts as a substrate for enzymes such as chymotrypsin or trypsin.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 163.17 g/mol
• Formel: C₉H₉NO₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C9H9NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-4,8,10H,5H2,(H,11,12)/t8-/m0/s1
• InChI Key: InChIKey=QNRXNRGSOJZINA-QMMMGPOBSA-N
• SMILES: O=C(O)[C@@H]1Cc2ccccc2N1