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· · COA & SDS available for every product · Same-day shipping on in-stock items viquidacin - Moligand™ , CAS No.904302-98-3
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. Synonyms
Viquidacin | 3-PIPERIDINECARBOXYLIC ACID, 4-((3S)-3-(3-FLUORO-6-METHOXY-4-QUINOLINYL)-3-HYDROXYPROPYL)-1-(2-(2-THIENYLTHIO)ETHYL)-, (3R,4R)- | 0TA0YE45QE | 3-Piperidinecarboxylic acid, 4-[(3S)-3-(3-fluoro-6-methoxy-4-quinolinyl)-3-hydroxypropyl]-1-[2-(2-t
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Why this grade Moligand™ Moligand™ 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 Synonyms
Viquidacin | 3-PIPERIDINECARBOXYLIC ACID, 4-((3S)-3-(3-FLUORO-6-METHOXY-4-QUINOLINYL)-3-HYDROXYPROPYL)-1-(2-(2-THIENYLTHIO)ETHYL)-, (3R, 4R)- | 0TA0YE45QE | 3-Piperidinecarboxylic acid, 4-[(3S)-3-(3-fluoro-6-methoxy-4-quinolinyl)-3-hydroxypropyl]-1-[2-(2-t
Specifications & Purity
Moligand™
Names and Identifiers Canonical Smiles COc1ccc2c(c1)c([C@H](CC[C@@H]1CCN(C[C@@H]1C(=O)O)CCSc1cccs1)O)c(cn2)F IUPAC Name (3R,4R)-4-[(3S)-3-(3-fluoro-6-methoxyquinolin-4-yl)-3-hydroxypropyl]-1-(2-thiophen-2-ylsulfanylethyl)piperidine-3-carboxylic acid InChIKey USGHRRVFKSLEJT-WVBUVRCRSA-N INCHI 1S/C25H29FN2O4S2/c1-32-17-5-6-21-18(13-17)24(20(26)14-27-21)22(29)7-4-16-8-9-28(15-19(16)25(30)31)10-12-34-23-3-2-11-33-23/h2-3,5-6,11,13-14,16,19,22,29H,4,7-10,12,15H2,1H3,(H,30,31)/t16-,19+,22+/m1/s1 Isomeric SMILES COC1=CC2=C(C(=CN=C2C=C1)F)[C@H](CC[C@@H]3CCN(C[C@@H]3C(=O)O)CCSC4=CC=CS4)O PubChem CID 11591505
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 4-quinolinemethanols Intermediate Tree Nodes Not available Direct Parent 4-quinolinemethanols Alternative Parents Haloquinolines Piperidinecarboxylic acids Anisoles Alkyl aryl ethers Alkylarylthioethers Aralkylamines Pyridines and derivatives Aryl fluorides Thiophenes Heteroaromatic compounds Trialkylamines Secondary alcohols Amino acids Carboxylic acids Azacyclic compounds Sulfenyl compounds Monocarboxylic acids and derivatives Organic oxides Carbonyl compounds Organofluorides Aromatic alcohols Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 4-quinolinemethanol - Haloquinoline - Piperidinecarboxylic acid - Aryl thioether - Anisole - Phenol ether - Alkyl aryl ether - Alkylarylthioether - Aralkylamine - Aryl fluoride - Aryl halide - Piperidine - Pyridine - Benzenoid - Thiophene - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Amino acid - Azacycle - Thioether - Sulfenyl compound - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Aromatic alcohol - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic nitrogen compound - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 4-quinolinemethanols. These are organoheterocyclic compounds containing a quinoline moiety substituted at the 4-position with a methanol. 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 504.600 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 10 Exact Mass 504.155 Da Monoisotopic Mass 504.155 Da Topological Polar Surface Area 136.000 Ų Heavy Atom Count 34 Formal Charge 0 Complexity 662.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 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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