Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| ALogP | 4.4 |
|---|
| Pubchem Sid | 488187811 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187811 |
| Sonrisas canónicas | CCOC(=O)C1=C(N(C2=CC(=C(C(=C21)CN(C)C)O)Br)C)CSC3=CC=CC=C3 |
| IUPAC Name | ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate |
| InChIKey | KCFYEAOKVJSACF-UHFFFAOYSA-N |
| INCHI | 1S/C22H25BrN2O3S/c1-5-28-22(27)20-18(13-29-14-9-7-6-8-10-14)25(4)17-11-16(23)21(26)15(19(17)20)12-24(2)3/h6-11,26H,5,12-13H2,1-4H3 |
| Isómeros SMILES | CCOC(=O)C1=C(N(C2=CC(=C(C(=C21)CN(C)C)O)Br)C)CSC3=CC=CC=C3 |
| Peso molecular | 477.43 |
| Reaxy-Rn | 5458019 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5458019&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| 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 | Hydroxyindoles N-alkylindoles Indoles Thiophenol ethers Pyrrole carboxylic acids and derivatives O-bromophenols Alkylarylthioethers Aralkylamines Aryl bromides Benzene and substituted derivatives N-methylpyrroles Vinylogous amides Heteroaromatic compounds Trialkylamines Amino acids and derivatives Carboxylic acid esters Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Organobromides Organooxygen compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indolecarboxylic acid derivative - N-alkylindole - Hydroxyindole - Indole - 2-bromophenol - Aryl thioether - Pyrrole-3-carboxylic acid or derivatives - Thiophenol ether - Alkylarylthioether - Aralkylamine - Aryl bromide - Substituted pyrrole - N-methylpyrrole - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyrrole - Vinylogous amide - Heteroaromatic compound - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Carboxylic acid ester - Carboxylic acid derivative - Azacycle - Sulfenyl compound - Monocarboxylic acid or derivatives - Thioether - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organic oxide - Organosulfur compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen 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 |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jul 03, 2024 | A299594 | |
| Certificate of Analysis | Jan 30, 2024 | A299594 | |
| Certificate of Analysis | Jun 01, 2023 | A299594 | |
| Certificate of Analysis | Feb 15, 2023 | A299594 |
| Peso molecular | 477.400 g/mol |
|---|---|
| XLogP3 | 4.400 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 8 |
| Exact Mass | 476.077 Da |
| Monoisotopic Mass | 476.077 Da |
| Topological Polar Surface Area | 80.000 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 546.000 |
| 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 |
| 1. Ting Zhang, Ge Bai, Nan Cai, Yongqian Lei, Pengran Guo, Jingwei Xu. (2023) The carbon-doped Fe3O4 montmorillonite particle electrode for the degradation of antiviral drugs in electro-Fenton system. APPLIED CLAY SCIENCE, [PMID:] [10.1016/j.clay.2023.107056] |
| 2. Hongrui Yang, Chen Wang, Wenjuan Zhu, Xia Zhang, Tiemei Li, Jing Fan. (2022) A Sustainable Strategy for Solid-Phase Extraction of Antiviral Drug from Environmental Waters by Immobilized Hydrogen Bond Acceptor. Nanomaterials, 12 (8): (1287). [PMID:35457995] [10.3390/nano12081287] |
| 3. Dai Tianming, Wang Min, Wang Pengzhen, Dai Libing, Dai Renke, Meng Qingqi. (2021) Inhibition effects of eight anti-coronavirus drugs on glycosides metabolism and glycosidases in human gut microflora. PHARMAZIE, 76 (5): (195-201). [PMID:33964992] [10.1691/ph.2021.01005] |
| 4. Cheng Chen, Bo-Han Li, Chao-Yu Wang, Er-Long Wang, Tian-Qiang Liu, Zhe Zhao. (2026) Umifenovir protects Procambarus clarkii against white spot syndrome virus by suppressing viral replication and modulating innate immunity. FISH & SHELLFISH IMMUNOLOGY, [PMID:41687754] [10.1016/j.fsi.2026.111206] |
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