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· · COA & SDS available for every product · Same-day shipping on in-stock items NNC 63-0532 - ≥98%(HPLC) , CAS No.250685-44-0
Synonyms
(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8-triaza-spiro[4.5]dec-3-yl)-acetic acid methyl ester | AQMPIDSGLFVVPL-UHFFFAOYSA-N | UNII-73663SY1DT | 73663SY1DT | J-015801 | (8-naphtalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8-triaza-spiro[4.5]dec-3-yl)-acetic acid
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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
(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1, 3, 8-triaza-spiro[4.5]dec-3-yl)-acetic acid methyl ester | AQMPIDSGLFVVPL-UHFFFAOYSA-N | UNII-73663SY1DT | 73663SY1DT | J-015801 | (8-naphtalen-1-ylmethyl-4-oxo-1-phenyl-1, 3, 8-triaza-spiro[4.5]dec-3-yl)-acetic acid
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Potent non-peptide agonist for the NOP receptor (EC50= 305 nM, Ki= 7.3 nM); ~ 12-fold selective over other receptors. Centrally active following systemic administrationin vivo.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles COC(=O)CN1CN(C2(C1=O)CCN(CC2)CC3=CC=CC4=CC=CC=C43)C5=CC=CC=C5 IUPAC Name methyl 2-[8-(naphthalen-1-ylmethyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl]acetate InChIKey AQMPIDSGLFVVPL-UHFFFAOYSA-N INCHI 1S/C27H29N3O3/c1-33-25(31)19-29-20-30(23-11-3-2-4-12-23)27(26(29)32)14-16-28(17-15-27)18-22-10-7-9-21-8-5-6-13-24(21)22/h2-13H,14-20H2,1H3 Isomeric SMILES COC(=O)CN1CN(C2(C1=O)CCN(CC2)CC3=CC=CC4=CC=CC=C43)C5=CC=CC=C5 Molecular Weight 443.54 Reaxy-Rn 13750987 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13750987&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 Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acid esters Alternative Parents Phenylimidazolidines Naphthalenes Azaspirodecane derivatives Aniline and substituted anilines Dialkylarylamines Aralkylamines Piperidines Imidazolidinones Tertiary carboxylic acid amides Methyl esters Trialkylamines Lactams Monocarboxylic acids and derivatives Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Alpha-amino acid ester - Phenylimidazolidine - Azaspirodecane - Naphthalene - Aniline or substituted anilines - Dialkylarylamine - Aralkylamine - Monocyclic benzene moiety - Imidazolidinone - Benzenoid - Piperidine - Imidazolidine - Methyl ester - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Lactam - Tertiary aliphatic amine - Tertiary amine - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. 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) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:ethanol, Max Conc. mg/mL: 2.22, Max Conc. mM: 5; Solvent:DMSO, Max Conc. mg/mL: 22.18, Max Conc. mM: 50 Molecular Weight 443.500 g/mol XLogP3 4.500 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 6 Exact Mass 443.221 Da Monoisotopic Mass 443.221 Da Topological Polar Surface Area 53.100 Ų Heavy Atom Count 33 Formal Charge 0 Complexity 699.000 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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