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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager PF-07038124 - Moligand™ , Inhibitor of phosphodiesterase 4B, CAS No.P612749, Inhibitor of phosphodiesterase 4B
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
GTPL11950 | (R)-4-(5-(4-Methoxy-3-propoxyphenyl)pyridin-3-yl)-1,2-oxaborolan-2-ol | M6ZU548FWD | US11559538, Example 4 | HY-144683 | PF 07038124 [WHO-DD] | 3-[(4R)-2-hydroxyoxaborolan-4-yl]-5-(4-methoxy-3-propoxyphenyl)pyridine | Pyridine, 3-((4R)-2-hydro
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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 Synonyme
GTPL11950 | (R)-4-(5-(4-Methoxy-3-propoxyphenyl)pyridin-3-yl)-1,2-oxaborolan-2-ol | M6ZU548FWD | US11559538, Example 4 | HY-144683 | PF 07038124 [WHO-DD] | 3-[(4R)-2-hydroxyoxaborolan-4-yl]-5-(4-methoxy-3-propoxyphenyl)pyridine | Pyridine, 3-((4R)-2-hydro
Spezifikationen & Reinheit
Moligand™
Mechanismus der Wirkung
Inhibitor of phosphodiesterase 4B
Namen und Kennungen Kanonisches Lächeln CCCOc1cc(ccc1OC)c1cncc(c1)[C@@H]1COB(O)C1 IUPAC Name 3-[(4R)-2-hydroxyoxaborolan-4-yl]-5-(4-methoxy-3-propoxyphenyl)pyridine InChIKey KXVKOYCGACSUPP-INIZCTEOSA-N INCHI 1S/C18H22BNO4/c1-3-6-23-18-8-13(4-5-17(18)22-2)14-7-15(11-20-10-14)16-9-19(21)24-12-16/h4-5,7-8,10-11,16,21H,3,6,9,12H2,1-2H3/t16-/m0/s1 Isomere SMILES B1(C[C@@H](CO1)C2=CN=CC(=C2)C3=CC(=C(C=C3)OC)OCCC)O PubChem CID 148293990
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 Klasse Pyridines and derivatives Subclass Phenylpyridines Intermediate Tree Nodes Not available Direct Parent Phenylpyridines Alternative Parents Phenoxy compounds Methoxybenzenes Anisoles Methylpyridines Hydroxypyridines Alkyl aryl ethers Oxaborole derivatives Heteroaromatic compounds Boronic acid esters Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic metalloid salts Azacyclic compounds Aldimines Organopnictogen compounds Organoboron compounds Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents 3-phenylpyridine - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Methylpyridine - Hydroxypyridine - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - 1,2-oxaborole derivative - Boronic acid ester - Boronic acid derivative - Oxacycle - Azacycle - Organic metalloid salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Ether - Aldimine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Organoboron compound - Imine - Aromatic heteromonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond. 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-Struktur Zugehörige Ziele (menschlich) Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Lösungsrechner 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 Bewertungen Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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