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224,000+ prodotti di ricerca · Triple ISO certified · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino Eseroline - ≥97,0% (HPLC) , CAS No.469-22-7 🧪
Why this grade ≥97,0% (HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Specifiche e purezza
≥97,0% (HPLC)
Condizioni di conservazione di stoccaggio
Room temperature
Nomi e identificatori Sorrisi canonici CC12CCN(C1N(C3=C2C=C(C=C3)O)C)C IUPAC Name (3aR,8bS)-3,4,8b-trimethyl-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-ol InChIKey HKGWQUVGHPDEBZ-OLZOCXBDSA-N INCHI 1S/C13H18N2O/c1-13-6-7-14(2)12(13)15(3)11-5-4-9(16)8-10(11)13/h4-5,8,12,16H,6-7H2,1-3H3/t12-,13+/m1/s1 Isomeri SMILES C[C@@]12CCN([C@@H]1N(C3=C2C=C(C=C3)O)C)C CAS alternativo 469-22-7 Termini MeSH eseroline;eseroline monohydrochloride, (3aS-cis)-isomer;eseroline, (+)-;eseroline, (3aR-cis)-isomer Reaxy-Rn 85274 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=85274&ln=
Documentazione 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Classe Indoles and derivatives Subclass Pyrroloindoles Intermediate Tree Nodes Not available Direct Parent Pyrroloindoles Alternative Parents Indoles Dialkylarylamines 1-hydroxy-2-unsubstituted benzenoids N-alkylpyrrolidines Pyrroles Azacyclic compounds Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Pyrroloindole - Indole - Dialkylarylamine - 1-hydroxy-2-unsubstituted benzenoid - N-alkylpyrrolidine - Benzenoid - Pyrrole - Pyrrolidine - Azacycle - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound Descrizione This compound belongs to the class of organic compounds known as pyrroloindoles. These are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. External Descriptors phenols - pyrroloindole Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Peso molecolare 218.290 g/mol XLogP3 0.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 0 Exact Mass 218.142 Da Monoisotopic Mass 218.142 Da Topological Polar Surface Area 26.700 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 296.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 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
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