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· · COA & SDS available for every product · Same-day shipping on in-stock items L-690,330 - Moligand™ , CAS No.142523-38-4
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
NILUTAMIDE (EP MONOGRAPH) | BRD-K28470988-001-01-2 | SR-01000597623-1 | J-007663 | Phosphonic acid, (1-(4-hydroxyphenoxy)ethylidene)bis- | [1-(4-Hydroxyphenoxy)ethylidene]bisphosphonic acid | HMS3411O20 | SCHEMBL9663413 | CAS-4394-00-7 | SR-01000597623 |
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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 Normal 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
NILUTAMIDE (EP MONOGRAPH) | BRD-K28470988-001-01-2 | SR-01000597623-1 | J-007663 | Phosphonic acid, (1-(4-hydroxyphenoxy)ethylidene)bis- | [1-(4-Hydroxyphenoxy)ethylidene]bisphosphonic acid | HMS3411O20 | SCHEMBL9663413 | CAS-4394-00-7 | SR-01000597623 |
Specifications & Purity
Moligand™
Biochemical and Physiological Mechanisms
A potent inhibitor of inositol monophophatase; stable to hydrolysis. Induces autophagy in COS-7 cells independently of mTOR inhibition.
Names and Identifiers Canonical Smiles CC(OC1=CC=C(C=C1)O)(P(=O)(O)O)P(=O)(O)O IUPAC Name [1-(4-hydroxyphenoxy)-1-phosphonoethyl]phosphonic acid InChIKey JKOCAAWWDVHWKB-UHFFFAOYSA-N INCHI 1S/C8H12O8P2/c1-8(17(10,11)12,18(13,14)15)16-7-4-2-6(9)3-5-7/h2-5,9H,1H3,(H2,10,11,12)(H2,13,14,15) Isomeric SMILES CC(OC1=CC=C(C=C1)O)(P(=O)(O)O)P(=O)(O)O Molecular Weight 298.13 Reaxy-Rn 7716207 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7716207&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 Organic acids and derivatives Class Organic phosphonic acids and derivatives Subclass Bisphosphonates Intermediate Tree Nodes Not available Direct Parent Bisphosphonates Alternative Parents 4-alkoxyphenols Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids Organic phosphonic acids Organopnictogen compounds Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents 4-alkoxyphenol - Bisphosphonate - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Organophosphonic acid - Organic oxygen compound - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Organic oxide - Organopnictogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as bisphosphonates. These are organic compounds containing two phosphonate groups linked together through a carbon atoms. 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 Solubility Solvent:water, Max Conc. mg/mL: 29.81, Max Conc. mM: 100 with gentle warming Molecular Weight 298.120 g/mol XLogP3 -1.700 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 4 Exact Mass 298.001 Da Monoisotopic Mass 298.001 Da Topological Polar Surface Area 145.000 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 355.000 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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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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