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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 8-Azabicyclo(3.2.1]octane, 3-(3,4-dichlorophenyl)-2-(methoxymethyl)-8-methyl-, (1R,2R,3S,5S)- , Monoamine transporter inhibitor, CAS No.195875-68-4, Monoamine transporter inhibitor
Synonyms
NS-2359 | 8-AZABICYCLO(3.2.1)OCTANE, 3-(3,4-DICHLOROPHENYL)-2-(METHOXYMETHYL)-8-METHYL-, (1R,2R,3S,5S)- | UNII-76H76554PA | DB05805 | GSK-372475 | CHEMBL4297385 | NS 2359 | NS2359 | SCHEMBL2996257 | GSK 372475 | AKOS040747612 | PGYDXVBZYKQYCS-VPWBDBDCSA-N
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Why this grade 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 Sinónimos
NS-2359 | 8-AZABICYCLO(3.2.1)OCTANE, 3-(3, 4-DICHLOROPHENYL)-2-(METHOXYMETHYL)-8-METHYL-, (1R, 2R, 3S, 5S)- | UNII-76H76554PA | DB05805 | GSK-372475 | CHEMBL4297385 | NS 2359 | NS2359 | SCHEMBL2996257 | GSK 372475 | AKOS040747612 | PGYDXVBZYKQYCS-VPWBDBDCSA-N
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Monoamine transporter inhibitor
Propiedades del producto Nombres e identificadores Sonrisas canónicas CN1C2CCC1C(C(C2)C3=CC(=C(C=C3)Cl)Cl)COC IUPAC Name (1R,2R,3S,5S)-3-(3,4-dichlorophenyl)-2-(methoxymethyl)-8-methyl-8-azabicyclo[3.2.1]octane InChIKey PGYDXVBZYKQYCS-VPWBDBDCSA-N INCHI 1S/C16H21Cl2NO/c1-19-11-4-6-16(19)13(9-20-2)12(8-11)10-3-5-14(17)15(18)7-10/h3,5,7,11-13,16H,4,6,8-9H2,1-2H3/t11-,12+,13+,16+/m0/s1 Isómeros SMILES CN1[C@H]2CC[C@@H]1[C@@H]([C@H](C2)C3=CC(=C(C=C3)Cl)Cl)COC Peso molecular 314.2 Reaxy-Rn 11758788 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11758788&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 Alkaloids and derivatives Clase Tropane alkaloids Subclass Phenyltropanes Intermediate Tree Nodes Not available Direct Parent Phenyltropanes Alternative Parents Phenylpiperidines Dichlorobenzenes Aralkylamines N-alkylpyrrolidines Aryl chlorides Trialkylamines Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organochlorides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenyltropane - Phenylpiperidine - 1,2-dichlorobenzene - Aralkylamine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Organic nitrogen compound - Organopnictogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenyltropanes. These are compounds containing a phenyl group linked to a tropane moiety. Tropane is an organonitrogenous [3.2.1] bicyclic organic compound. 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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