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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Cearoin - Moligand™,≥98% , CAS No.52811-37-7
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. ≥98% Synonyms
SDCCGMLS-0066944.P001 | Spectrum5_000314 | KBio2_006208 | KBioSS_001072 | (2,5-dihydroxy-4-methoxyphenyl)(phenyl)methanone | DivK1c_006214 | AKOS040761474 | NCGC00095562-02 | KBio3_002189 | BRD-K20420220-001-03-9 | HY-N8418 | Spectrum_000592 | SpecPlus_00
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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.
Descripción general Cearoin increases autophagy and apoptosis through the production of ROS and the activation of ERK.
Specifications Sinónimos
SDCCGMLS-0066944.P001 | Spectrum5_000314 | KBio2_006208 | KBioSS_001072 | (2, 5-dihydroxy-4-methoxyphenyl)(phenyl)methanone | DivK1c_006214 | AKOS040761474 | NCGC00095562-02 | KBio3_002189 | BRD-K20420220-001-03-9 | HY-N8418 | Spectrum_000592 | SpecPlus_00
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Cearoin increases autophagy and apoptosis through the production of ROS and the activation of ERK.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas COC1=C(C=C(C(=C1)O)C(=O)C2=CC=CC=C2)O IUPAC Name (2,5-dihydroxy-4-methoxyphenyl)-phenylmethanone InChIKey NFJVELXCUBWAFL-UHFFFAOYSA-N INCHI 1S/C14H12O4/c1-18-13-8-11(15)10(7-12(13)16)14(17)9-5-3-2-4-6-9/h2-8,15-16H,1H3 Isómeros SMILES COC1=C(C=C(C(=C1)O)C(=O)C2=CC=CC=C2)O CAS alternativo 52811-37-7 PubChem CID 3938139 Términos de entrada MeSH 2,5-dihydroxy-4-methoxybenzophenone;5-OH-BP-3 compound Peso molecular 244.24
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 Benzenoids Clase Benzene and substituted derivatives Subclass Benzophenones Intermediate Tree Nodes Not available Direct Parent Benzophenones Alternative Parents Diphenylmethanes Aryl-phenylketones Methoxyphenols Phenoxy compounds Methoxybenzenes Hydroquinones Benzoyl derivatives Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Benzophenone - Diphenylmethane - Aryl-phenylketone - Methoxyphenol - Anisole - Phenoxy compound - Benzoyl - Hydroquinone - Phenol ether - Aryl ketone - Methoxybenzene - Alkyl aryl ether - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Ketone - Ether - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad DMSO : 50 mg/mL (204.72 mM; Need ultrasonic) Sensibilidad light sensitive; air sensitive Peso molecular 244.240 g/mol XLogP3 3.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 244.074 Da Monoisotopic Mass 244.074 Da Topological Polar Surface Area 66.800 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 286.000 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 Reseñas 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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