Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ramelteon is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.
a melatonin MT1/MT2 receptor agonist.
| ALogP | 2.7 |
|---|
| Pubchem Sid | 504757839 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504757839 |
| Sonrisas canónicas | CCC(=O)NCCC1CCC2=C1C3=C(C=C2)OCC3 |
| IUPAC Name | N-[2-[(8S)-2,6,7,8-tetrahydro-1H-cyclopenta[e][1]benzofuran-8-yl]ethyl]propanamide |
| InChIKey | YLXDSYKOBKBWJQ-LBPRGKRZSA-N |
| INCHI | 1S/C16H21NO2/c1-2-15(18)17-9-7-12-4-3-11-5-6-14-13(16(11)12)8-10-19-14/h5-6,12H,2-4,7-10H2,1H3,(H,17,18)/t12-/m0/s1 |
| Isómeros SMILES | CCC(=O)NCC[C@@H]1CCC2=C1C3=C(C=C2)OCC3 |
| WGK Alemania | 2 |
| PubChem CID | 208902 |
| Peso molecular | 259.34 |
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 | Benzenoids |
| Clase | Indanes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indanes |
| Alternative Parents | Coumarans Alkyl aryl ethers Secondary carboxylic acid amides Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indane - Coumaran - Alkyl aryl ether - Carboxamide group - Secondary carboxylic acid amide - Oxacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as indanes. These are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring. |
| 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 | Dec 10, 2025 | R125051 | |
| Certificate of Analysis | Apr 16, 2025 | R125051 | |
| Certificate of Analysis | Jan 25, 2023 | R125051 | |
| Certificate of Analysis | Jan 11, 2023 | R125051 |
| Solubilidad | Solvent:DMSO, Max Conc. mg/mL: 25.93, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 25.93, Max Conc. mM: 100 |
|---|---|
| Rotación específica [α] | -57° (C=1,CHCl3) |
| Punto de inflamación (°F) | 35.6 °F |
| Punto de inflamación (°C) | 35.6°F |
| Punto de fusión (°C) | 116 °C |
| Peso molecular | 259.339 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | 259.157 Da |
| Monoisotopic Mass | 259.157 Da |
| Topological Polar Surface Area | 38.300 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 331.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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. Wang Guijie, Tian Fang, Li Yu, Liu Yang, Liu Chunfeng. (2021) Ramelteon Mitigates Free Fatty Acid (FFA)–Induced Attachment of Monocytes to Brain Vascular Endothelial Cells. NEUROTOXICITY RESEARCH, 39 (6): (1937-1945). [PMID:34792763] [10.1007/s12640-021-00422-1] |
Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →