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· · COA & SDS available for every product · Same-day shipping on in-stock items AZ12971554 - Moligand™ , Inhibitor of coagulation factor II; thrombin, CAS No.A607832, Inhibitor of coagulation factor II; thrombin
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
(5S)-N-[5-Chloro-2-(1H-tetrazol-1-yl)benzyl]-1-[(2R)-2-(4-fluorophenyl)-2-hydroxyacetyl]-4,5-dihydro-1H-pyrazole-5-carboxamide | GMKHQRCPNMGCIX-ZWKOTPCHSA-N | SCHEMBL642384 | (5S)-N-{[5-chloro-2-(1H-1,2,3,4-tetrazol-1-yl)phenyl]methyl}-1-[(2R)-2-(4-fluoro
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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
(5S)-N-[5-Chloro-2-(1H-tetrazol-1-yl)benzyl]-1-[(2R)-2-(4-fluorophenyl)-2-hydroxyacetyl]-4, 5-dihydro-1H-pyrazole-5-carboxamide | GMKHQRCPNMGCIX-ZWKOTPCHSA-N | SCHEMBL642384 | (5S)-N-{[5-chloro-2-(1H-1, 2, 3, 4-tetrazol-1-yl)phenyl]methyl}-1-[(2R)-2-(4-fluoro
Specifications & Purity
Moligand™
Mechanism of action
Inhibitor of coagulation factor II; thrombin
Names and Identifiers Canonical Smiles O=C([C@@H]1CC=NN1C(=O)[C@@H](c1ccc(cc1)F)O)NCc1cc(Cl)ccc1n1cnnn1 IUPAC Name (5S)-N-{[5-chloro-2-(1H-1,2,3,4-tetrazol-1-yl)phenyl]methyl}-1-[(2R)-2-(4-fluorophenyl)-2-hydroxyacetyl]-4,5-dihydro-1H-pyrazole-5-carboxamide InChIKey GMKHQRCPNMGCIX-ZWKOTPCHSA-N INCHI 1S/C20H17ClFN7O3/c21-14-3-6-16(28-11-24-26-27-28)13(9-14)10-23-19(31)17-7-8-25-29(17)20(32)18(30)12-1-4-15(22)5-2-12/h1-6,8-9,11,17-18,30H,7,10H2,(H,23,31)/t17-,18+/m0/s1 Isomeric SMILES C1C=NN([C@@H]1C(=O)NCC2=C(C=CC(=C2)Cl)N3C=NN=N3)C(=O)[C@@H](C4=CC=C(C=C4)F)O PubChem CID 44537923
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 Azoles Subclass Tetrazoles Intermediate Tree Nodes Not available Direct Parent Phenyltetrazoles and derivatives Alternative Parents Phenylacetamides Alpha amino acids and derivatives Fluorobenzenes Chlorobenzenes Aryl chlorides Aryl fluorides Pyrazolines Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols N-alkylated hydrazones Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides Aromatic alcohols Organofluorides Molecular Framework Aromatic heteromonocyclic compounds Substituents Phenyltetrazole - Alpha-amino acid or derivatives - Phenylacetamide - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrazoline - Carboxamide group - N-alkylated hydrazone - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Azacycle - Organochloride - Organohalogen compound - Aromatic alcohol - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as phenyltetrazoles and derivatives. These are compounds containing a phenyltetrazole skeleton, which consists of a tetrazole bound to 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) Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
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