≥98% 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.
Used in an efficient synthesis of fused pyrroloquinolinedicarboxylates from acetylenedicarboxylates and triphenylphosphine. 1.reactant for preparation of antiandrogens. 2.reactant for preparation of antiplatelet agent. 3.reactant for preparation of liver X receptor (LXR) agonists. 4.reactant for preparation of antagonists of the EP3 receptor for prostaglandin E2. 5.reactant for preparation of inhibitors of glycoprotein perforin. 6.reactant for preparation of potent antitubulin agents. 7.reactant for preparation of potential insulin receptor activators. 8.reactant for preparation of potential scaffolds for peptide mimetics. 9.reactant for preparation of 5-Hydroxytryptamine1D receptor antagonist. 10.reactant for preparation of indolocarbazole kinase
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 | Indoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indoles |
| Alternative Parents | Aryl-aldehydes Benzenoids Vinylogous amides Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indole - Aryl-aldehyde - Benzenoid - Pyrrole - Vinylogous amide - Heteroaromatic compound - Azacycle - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 L2418054 | Certificate of Analysis | Sep 01, 2026 | I122940 |
| H2212299 | Certificate of Analysis | Feb 04, 2026 | I122940 |
| H2212306 | Certificate of Analysis | Feb 04, 2026 | I122940 |
| H2212344 | Certificate of Analysis | Feb 04, 2026 | I122940 |
| H2212494 | Certificate of Analysis | Feb 04, 2026 | I122940 |
| H2212495 | Certificate of Analysis | Feb 04, 2026 | I122940 |
| I1424087 | Certificate of Analysis | Dec 22, 2025 | I122940 |
| E1428003 | Certificate of Analysis | Nov 13, 2025 | I122940 |
| Empfindlichkeit | Air Sensitive;light sensitive |
|---|---|
| Schmelzpunkt (°C) | 86-89°C |
| Molekulargewicht | 145.160 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 145.053 Da |
| Monoisotopic Mass | 145.053 Da |
| Topological Polar Surface Area | 32.900 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 158.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
