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L-Octahydroindole-2-carboxylic acid, 98%|190551|80875-98-5

L-Octahydroindole-2-carboxylic acid, 98%

Cat. No JK190551_5_G
J&K Chemical

Product Information

Product Name
L-Octahydroindole-2-carboxylic acid, 98%
Brand Name
J&K
Product Number
190551
CAS
80875-98-5
Molecular Formula
C9H15NO2
Molecular Weight
169.22
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7408452
IUPAC Name
(2S,3aS,7aS)-2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylic acid
InChI Key
CQYBNXGHMBNGCG-FXQIFTODSA-N
SMILES
C1CCC@H2C@@H(C1)CC@H(N2)C(=O)O

Properties

Melting Point
268-271
Optical Activity
-50 to -46 (C=1, MeOH)

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Organocatalyzed Oxa-Diels–Alder Reactions: Recent Progress
Publication Name: Synthesis
Publication Date: 2021-07-13
DOI: 10.1055/a-1514-1049

Transition Metal Catalyzed Asymmetric Aryl Carbon–Heteroatom Bond Coupling Reactions
Publication Name: Synlett
Publication Date: 2016-01-27
DOI: 10.1055/s-0035-1560552

An Unexpected Inversion of Enantioselectivity in a Copper-Catalyzed Intramolecular­ Desymmetric Aryl C–N Coupling Reaction
Publication Name: Synthesis
Publication Date: 2014-05-09
DOI: 10.1055/s-0033-1338638

Inverse-Electron-Demand Hetero-Diels–Alder Reaction Using Modular Catalysts
Publication Name: Synfacts
Publication Date: 2013-06-17
DOI: 10.1055/s-0033-1339245

Organocatalyzed Michael Addition Reaction by Novel (2R,3aS,7aS)-Octa-hydroindole-2-carboxylic Acid, a New Fused Proline
Publication Name: Synlett
Publication Date: 2011-01
DOI: 10.1055/s-0030-1259296

L-Octahydroindole-2-carboxylic acid, 98%

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