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· · COA & SDS available for every product · Same-day shipping on in-stock items CU CPT 9a - 10mM in DMSO , CAS No.2165340-32-7
GRADE & PURITY 10mM in DMSO
Synonyms
4-(7-methoxyquinolin-4-yl)-2-methylphenol | 4-(7-methoxyquinolin-4-yl)-2-methyl-phenol | BS-16510 | s9730 | 2165340-32-7 | EX-A3051 | CU CPT 9a | HY-112667 | AC-36561 | 4-(7-Methoxy-4-quinolinyl)-2-methylphenol | 2-Methyl-4-(7-methoxy-4-quinolinyl)phenol
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 Synonyms
4-(7-methoxyquinolin-4-yl)-2-methylphenol | 4-(7-methoxyquinolin-4-yl)-2-methyl-phenol | BS-16510 | s9730 | 2165340-32-7 | EX-A3051 | CU CPT 9a | HY-112667 | AC-36561 | 4-(7-Methoxy-4-quinolinyl)-2-methylphenol | 2-Methyl-4-(7-methoxy-4-quinolinyl)phenol
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Potent TLR8 inhibitor (IC50= 0.5 nM and Kd= 21 nM). Stabilizes the TLR8 dimer in its resting state, preventing activation. Suppresses TLR8-mediated proinflammatory signaling in various cell lines and human primary cells.
CU-CPT9a is a potent and selective
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC1=C(C=CC(=C1)C2=C3C=CC(=CC3=NC=C2)OC)O IUPAC Name 4-(7-methoxyquinolin-4-yl)-2-methylphenol InChIKey HNYBTVKYLVLWCB-UHFFFAOYSA-N INCHI 1S/C17H15NO2/c1-11-9-12(3-6-17(11)19)14-7-8-18-16-10-13(20-2)4-5-15(14)16/h3-10,19H,1-2H3 Isomeric SMILES CC1=C(C=CC(=C1)C2=C3C=CC(=CC3=NC=C2)OC)O Molecular Weight 265.31 Reaxy-Rn 32065721 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=32065721&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 Phenylpyridines Ortho cresols Anisoles Toluenes Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenylquinoline - 4-phenylpyridine - O-cresol - Anisole - 1-hydroxy-2-unsubstituted benzenoid - Toluene - Phenol - Alkyl aryl ether - Benzenoid - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Azacycle - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - 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) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 265.310 g/mol XLogP3 3.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 265.11 Da Monoisotopic Mass 265.11 Da Topological Polar Surface Area 42.400 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 322.000 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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