82717-40-6

Basic information

• Product Name: 1H-Indole-2-carboxylicacid,octahydro-(9CI)
• Synonyms: 1H-Indole-2-carboxylicacid,octahydro-(9CI)
• CAS NO: 82717-40-6
• Molecular Formula: C₉H₁₅NO₂
• Molecular Weight: 169.2209
• Product Categories: PYRROLE
• Mol File: 82717-40-6.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 318.6±25.0 °C(Predicted)
• Appearance: /
• Density: 1.135±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 2.47±0.20(Predicted)
• CAS DataBase Reference: 1H-Indole-2-carboxylicacid,octahydro-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-2-carboxylicacid,octahydro-(9CI)(82717-40-6)
• EPA Substance Registry System: 1H-Indole-2-carboxylicacid,octahydro-(9CI)(82717-40-6)

Safety Data

• Hazardous Substances Data: 82717-40-6(Hazardous Substances Data)

Usage

General Description

1H-Indole-2-carboxylic acid, octahydro-(9CI), also known as tetrahydro-1H-indole-2-carboxylic acid, is a chemical compound with the molecular formula C10H13NO2. It is a derivative of indole, a heterocyclic aromatic organic compound. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals. It has also shown potential in the research and development of new drugs, particularly in the areas of neuroscience and psychiatry. It is important to handle this compound with care, as it may pose health hazards if not properly managed.

Upstream product

• 87624-03-1 (4aR,8aS)-3-Chloro-octahydro-quinolin-2-one 
• 87623-95-8 (2R,3aS,7aR)-1-Acetyl-octahydro-indole-2-carbonitrile 
• 89226-35-7 N-[(1S,2R)-2-(2-Chloro-2-cyano-ethyl)-cyclohexyl]-acetamide 
• 59224-99-6 trans-3,4,4a,5,6,7,8,8a-Octahydro-2(1H)-quinolinone 
• 87624-03-1 (4aS,8aS)-3-Chloro-octahydro-quinolin-2-one 
• 79799-08-9 (2S,3aS,7aS)-Octahydro-indole-2-carboxylic acid ethyl ester 
• 16851-56-2 indolin-2-yl carboxylic acid 
• 3770-50-1 2-carbethoxyindole 
• 4169-27-1 cis-3,4,4a,5,6,7,8,8a-Octahydro-2(1H)-quinolinone 
• 87623-95-8 (2S,3aR,7aR)-1-Acetyl-octahydro-indole-2-carbonitrile 
• 120-72-9 indole 
• 87623-93-6 (3aR,7aR)-1-(Octahydro-indol-1-yl)-ethanone 
• 1193-68-6 cis-octahydroindole 
• 281190-60-1 trans-1-amino-2-(2,2-dimethoxyethyl)-cyclohexane 

Downstream Products

• 108395-25-1 (2α,3aβ,7aβ)-1-(3-bromobenzoyl)octahydro-1H-indole-2-carboxylic acid 
• 80828-12-2 (2R,3aR,7aR)-1-(3-Acetylsulfanyl-propionyl)-octahydro-indole-2-carboxylic acid 
• 80828-15-5 (2α,3aβ,7aβ)-1-<3-(acetylthio)-2-methyl-1-oxopropyl>octahydro-1H-indole-2-carboxylic acid 
• 80828-15-5 (2R,3aR,7aR)-1-((S)-3-Acetylsulfanyl-2-methyl-propionyl)-octahydro-indole-2-carboxylic acid 
• 80828-31-5 (2α,3aβ,7aβ)-1-benzoyloctahydro-1H-indole-2-carboxylic acid 
• 80876-00-2 (2α,3aβ,7aβ)-octahydro-1H-indole-2-carboxylic acid 1,1-dimethylethyl ester 
• 82717-91-7 (+/-)-benzyl (2S,3aS,7aS)-octahydroindole-2-carboxylate p-toluenesulfonic acid salt 
• 960529-89-9 benzyl (2R,3aR,7aR)-N-(tert-butoxycarbonyl)octahydroindole-2-carboxylate 
• 960529-90-2 benzyl (2S,3aS,7aS)-N-(tert-butoxycarbonyl)octahydroindole-2-carboxylate 
• 109523-13-9 (2S,3aS,7aS)-1-(tert-butoxycarbonyl)octahydro-1H-indole-2-carboxylic acid 
• 80876-00-2 (2α,3aβ,7aβ)-octahydro-1H-indole-2-carboxylic acid tert-butyl ester 
• 80875-98-5 (2S,3aS,7aS)-perhydroindole-2-carboxylic acid 
• 80875-99-6 (2S,3aS,7aS)-1-Benzoyl-octahydro-indole-2-carboxylic acid 
• 108395-27-3 (6aα,10aα,11aα)-decahydro-1H,5H-<1,4>thiazepino<4,3-a>indole-1,5-dione 

Relevant articles and documents

Efficient access to N-protected derivatives of (R,R,R)- and (S,S,S)-octahydroindole-2-carboxylic acid by HPLC resolution

The preparation of the proline analogue (2S,3aS,7aS)-octahydroindole-2-carboxylic acid (Oic) and its enantiomer, (2R,3aR,7aR)-Oic, is described. A racemic precursor has been synthesized in good yield and subjected to HPLC resolution on a chiral column. The high efficiency of both the synthetic and chromatographic procedures has allowed the isolation of multigram quantities of each amino acid in enantiomerically pure form and suitably protected for use in peptide synthesis.

Decahydroisoquinoline carboxylic acids

What are disclosed are aminoacid compounds of the formula STR1 wherein n is 0 or 1, and salts thereof, said compounds and salts having hypotensive properties; methods for making the compounds; pharmaceutical compositions containing the compounds or salts;

Antiglaucoma compositions and methods

The present invention relates to ophthalmological pharmaceutical compositions comprising (benzothiadiazine, benzamide and benzenesulfonyl)phenyl-substituted carboxyalkyl dipeptide compounds and to methods for using said composition in reducing intraocular