≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Reactant for enantioselective α-amination reactions;Reactant for aldol reaction with glyoxal derivatives;Reactant for amine thiourea catalyzed conjugate addition to α,β-unsaturated aldehydes;Reactant for O-acetylation reactions;Reactant for preparation of a disubstituted oxoindole by using rhodium-catalyzed cyclopropanation/ring-opening reactions.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Klasse | Indoles and derivatives |
| Subclass | Indolines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indolines |
| Alternative Parents | Benzenoids Secondary carboxylic acid amides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Dihydroindole - Benzenoid - Carboxamide group - Lactam - Secondary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Aromatic heteropolycyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. |
| External Descriptors | a small molecule |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 H1623043 | Certificate of Analysis | Apr 02, 2024 | M115491 |
| E2308837 | Certificate of Analysis | Feb 20, 2023 | M115491 |
| E2308885 | Certificate of Analysis | Feb 20, 2023 | M115491 |
| I2512589 | Certificate of Analysis | Feb 20, 2023 | M115491 |
| E1907050 | Certificate of Analysis | Feb 09, 2023 | M115491 |
| E2308841 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| E2308851 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| E2308853 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| E2308873 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| E2308877 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| E2308882 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| L2508744 | Certificate of Analysis | Jan 16, 2023 | M115491 |
| Löslichkeit | Insoluble in water. |
|---|---|
| Schmelzpunkt (°C) | 117-121°C |
| Molekulargewicht | 147.170 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 147.068 Da |
| Monoisotopic Mass | 147.068 Da |
| Topological Polar Surface Area | 29.100 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 178.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
