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· · COA & SDS available for every product · Same-day shipping on in-stock items ELQ-300 - Moligand™, ≥98% , CAS No.1354745-52-0
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
6-Chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)-4(1H)-quinolinone | 6-chloro-7-methoxy-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-1H-quinolin-4-one | 4(1H)-Quinolinone, 6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)ph
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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.
Overview Information
ELQ-300, a bioavailable antimalarial agent, is a potent and orally inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
Specifications Synonyms
6-Chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)-4(1H)-quinolinone | 6-chloro-7-methoxy-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-1H-quinolin-4-one | 4(1H)-Quinolinone, 6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)ph
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
ELQ-300, a bioavailable antimalarial agent, is a potent and orally inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC1=C(C(=O)C2=CC(=C(C=C2N1)OC)Cl)C3=CC=C(C=C3)OC4=CC=C(C=C4)OC(F)(F)F IUPAC Name 6-chloro-7-methoxy-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-1H-quinolin-4-one InChIKey WZDNKHCQIZRDKW-UHFFFAOYSA-N INCHI 1S/C24H17ClF3NO4/c1-13-22(23(30)18-11-19(25)21(31-2)12-20(18)29-13)14-3-5-15(6-4-14)32-16-7-9-17(10-8-16)33-24(26,27)28/h3-12H,1-2H3,(H,29,30) Isomeric SMILES CC1=C(C(=O)C2=CC(=C(C=C2N1)OC)Cl)C3=CC=C(C=C3)OC4=CC=C(C=C4)OC(F)(F)F Molecular Weight 475.85 Reaxy-Rn 26906802 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=26906802&ln=
Documentation 📋 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 Class Quinolines and derivatives Subclass Phenylquinolines Intermediate Tree Nodes Not available Direct Parent Phenylquinolines Alternative Parents Diphenylethers Phenylpyridines Chloroquinolines Diarylethers Hydroquinolones Hydroquinolines Phenoxy compounds Anisoles Methylpyridines Alkyl aryl ethers Aryl chlorides Heteroaromatic compounds Vinylogous amides Trihalomethanes Azacyclic compounds Organochlorides Organic oxides Organonitrogen compounds Hydrocarbon derivatives Alkyl fluorides Organofluorides Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenylquinoline - Diphenylether - 3-phenylpyridine - Diaryl ether - Haloquinoline - Dihydroquinolone - Chloroquinoline - Dihydroquinoline - Anisole - Phenoxy compound - Phenol ether - Alkyl aryl ether - Methylpyridine - Benzenoid - Pyridine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Vinylogous amide - Heteroaromatic compound - Trihalomethane - Azacycle - Ether - Organofluoride - Organochloride - Organohalogen compound - Organic oxide - Organic oxygen compound - Organooxygen compound - Halomethane - Alkyl fluoride - Organic nitrogen compound - Alkyl halide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group. External Descriptors Not available 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 475.800 g/mol XLogP3 6.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 5 Exact Mass 475.08 Da Monoisotopic Mass 475.08 Da Topological Polar Surface Area 56.800 Ų Heavy Atom Count 33 Formal Charge 0 Complexity 730.000 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
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