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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items tunlametinib - Moligand™ , CAS No.1801756-06-8
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
6-Benzothiazolecarboxamide, 4-fluoro-5-((2-fluoro-4-iodophenyl)amino)-N-(2-hydroxyethoxy)- | UFZJUVFSSINETF-UHFFFAOYSA-N | HL085 | HL-085 | Hl 085 | Example 9 [WO2013107283A1] | tunlametinib | HY-132844 | HL 085 [WHO-DD] | UNII-IF25NR1PV3 | Tunlametinib [
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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
6-Benzothiazolecarboxamide, 4-fluoro-5-((2-fluoro-4-iodophenyl)amino)-N-(2-hydroxyethoxy)- | UFZJUVFSSINETF-UHFFFAOYSA-N | HL085 | HL-085 | Hl 085 | Example 9 [WO2013107283A1] | tunlametinib | HY-132844 | HL 085 [WHO-DD] | UNII-IF25NR1PV3 | Tunlametinib [
Specifications & Purity
Moligand™
Names and Identifiers Canonical Smiles
Fc1c(c(cc2c1ncs2)C(=O)NOCCO)Nc1c(cc(cc1)I)F
IUPAC Name
4-fluoro-5-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)-1,3-benzothiazole-6-carboxamide
InChIKey
UFZJUVFSSINETF-UHFFFAOYSA-N
INCHI
1S/C16H12F2IN3O3S/c17-10-5-8(19)1-2-11(10)21-14-9(16(24)22-25-4-3-23)6-12-15(13(14)18)20-7-26-12/h1-2,5-7,21,23H,3-4H2,(H,22,24)
Isomeric SMILES
C1=CC(=C(C=C1I)F)NC2=C(C3=C(C=C2C(=O)NOCCO)SC=N3)F
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 Benzothiazoles Subclass Not available Intermediate Tree Nodes Not available Direct Parent Benzothiazoles Alternative Parents Aniline and substituted anilines Iodobenzenes Fluorobenzenes Aryl iodides Aryl fluorides Vinylogous amides Thiazoles Heteroaromatic compounds Amino acids and derivatives Secondary amines Azacyclic compounds Primary alcohols Organopnictogen compounds Organoiodides Organofluorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 1,3-benzothiazole - Aniline or substituted anilines - Iodobenzene - Halobenzene - Fluorobenzene - Benzenoid - Monocyclic benzene moiety - Aryl iodide - Aryl halide - Aryl fluoride - Heteroaromatic compound - Vinylogous amide - Thiazole - Azole - Amino acid or derivatives - Azacycle - Secondary amine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organoiodide - Organofluoride - Organohalogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as benzothiazoles. These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom). 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.
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