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· · COA & SDS available for every product · Same-day shipping on in-stock items SB 207710 - Moligand™ , Antagonist of 5-HT 4 receptor;Antagonist of 5-HT 7 receptor, CAS No.S613439, Antagonist of 5-HT 4 receptor;Antagonist of 5-HT 7 receptor
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
(1-Butylpiperidin-4-yl)methyl 5-azanyl-6-iodanyl-2,3-dihydro-1,4-benzodioxine-8-carboxylate | L008862 | SCHEMBL2939430 | AKOS040749411 | QWZ4KZ6JHE | 8-Amino-7-iodo-2,3-dihydro-benzo[1,4]dioxine-5-carboxylic acid 1-butyl-piperidin-4-ylmethyl ester | GTPL2
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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
(1-Butylpiperidin-4-yl)methyl 5-azanyl-6-iodanyl-2, 3-dihydro-1, 4-benzodioxine-8-carboxylate | L008862 | SCHEMBL2939430 | AKOS040749411 | QWZ4KZ6JHE | 8-Amino-7-iodo-2, 3-dihydro-benzo[1, 4]dioxine-5-carboxylic acid 1-butyl-piperidin-4-ylmethyl ester | GTPL2
Specifications & Purity
Moligand™
Mechanism of action
Antagonist of 5-HT 4 receptor;Antagonist of 5-HT 7 receptor
Names and Identifiers Canonical Smiles CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N IUPAC Name (1-butylpiperidin-4-yl)methyl 5-amino-6-iodo-2,3-dihydro-1,4-benzodioxine-8-carboxylate InChIKey FCKKCDRMGKXQDK-UHFFFAOYSA-N INCHI 1S/C19H27IN2O4/c1-2-3-6-22-7-4-13(5-8-22)12-26-19(23)14-11-15(20)16(21)18-17(14)24-9-10-25-18/h11,13H,2-10,12,21H2,1H3 Isomeric SMILES CCCCN1CCC(CC1)COC(=O)C2=CC(=C(C3=C2OCCO3)N)I PubChem CID 5311423
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 Class Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Aminobenzoic acids and derivatives Alternative Parents Benzo-1,4-dioxanes Alkyl aryl ethers Aryl iodides Para dioxins Piperidines Carboxylic acid esters Amino acids and derivatives Trialkylamines Monocarboxylic acids and derivatives Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Organoiodides Organic oxides Hydrocarbon derivatives Primary amines Molecular Framework Aromatic heteropolycyclic compounds Substituents Aminobenzoic acid or derivatives - Benzo-1,4-dioxane - Benzodioxane - Alkyl aryl ether - Aryl halide - Aryl iodide - Para-dioxin - Piperidine - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Organopnictogen compound - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organoiodide - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as aminobenzoic acids and derivatives. These are benzoic acids (or derivative thereof) containing an amine group attached to the benzene moiety. 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) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 474.300 g/mol XLogP3 3.500 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 474.102 Da Monoisotopic Mass 474.102 Da Topological Polar Surface Area 74.000 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 459.000 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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