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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items ITE - 10mM in DMSO , CAS No.448906-42-1
GRADE & PURITY 10mM in DMSO
Synonyms
2-[1H-indol-3-yl(oxo)methyl]-4-thiazolecarboxylic acid methyl ester | methyl 2-(1H-indole-3-carbonyl)thiazole-4-carboxylate | NCGC00159529-01 | BDBM50506039 | EX-A1251 | 2-(1'H-Indole-3'-carbonyl)-thiazole-4-carboxylic acid | A22724 | Q27164789 | MFCD0641
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 Sinónimos
2-[1H-indol-3-yl(oxo)methyl]-4-thiazolecarboxylic acid methyl ester | methyl 2-(1H-indole-3-carbonyl)thiazole-4-carboxylate | NCGC00159529-01 | BDBM50506039 | EX-A1251 | 2-(1'H-Indole-3'-carbonyl)-thiazole-4-carboxylic acid | A22724 | Q27164789 | MFCD0641
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Endogenous aryl hydrocarbon receptor (AhR) agonist (Ki = 3 nM). Enhances differentiation of cancer stem like cells detected by the decrease of sphere formation and proliferation from glioblastoma cells U87.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
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Nombres e identificadores Sonrisas canónicas COC(=O)C1=CSC(=N1)C(=O)C2=CNC3=CC=CC=C32 IUPAC Name methyl 2-(1H-indole-3-carbonyl)-1,3-thiazole-4-carboxylate InChIKey KDDXOGDIPZSCTM-UHFFFAOYSA-N INCHI 1S/C14H10N2O3S/c1-19-14(18)11-7-20-13(16-11)12(17)9-6-15-10-5-3-2-4-8(9)10/h2-7,15H,1H3 Isómeros SMILES COC(=O)C1=CSC(=N1)C(=O)C2=CNC3=CC=CC=C32 Peso molecular 286.31 Reaxy-Rn 9406816 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9406816&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 Organoheterocyclic compounds Clase Indoles and derivatives Subclass Indolecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Indolecarboxylic acids and derivatives Alternative Parents Indoles Thiazolecarboxylic acids and derivatives Aryl ketones 2,4-disubstituted thiazoles Substituted pyrroles Benzenoids Vinylogous amides Methyl esters Heteroaromatic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Indolecarboxylic acid derivative - Indole - Thiazolecarboxylic acid or derivatives - Aryl ketone - 2,4-disubstituted 1,3-thiazole - Substituted pyrrole - Benzenoid - Azole - Pyrrole - Heteroaromatic compound - Thiazole - Methyl ester - Vinylogous amide - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. These are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole. 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 Peso molecular 286.310 g/mol XLogP3 2.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 286.041 Da Monoisotopic Mass 286.041 Da Topological Polar Surface Area 100.000 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 404.000 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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