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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager FAUC-346 - ≥98% , CAS No.474432-65-0
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,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.
Übersicht Information
FAUC-346 is a highly selective agonist of D3 partial with EC50 of 1.5 nM. FAUC-346 also demonstrates an inhibitory effect on cocaine-seeking behavior.
Specifications Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
FAUC-346 is a highly selective agonist of D3 partial with EC50 of 1.5 nM. FAUC-346 also demonstrates an inhibitory effect on cocaine-seeking behavior.
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Pubchem Sid 528764443 Kanonisches Lächeln COC1=CC=CC=C1N2CCN(CC2)CCCCNC(=O)C3=CC4=CC=CC=C4S3 IUPAC Name N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-1-benzothiophene-2-carboxamide InChIKey KFMBPIZMZUDONQ-UHFFFAOYSA-N INCHI 1S/C24H29N3O2S/c1-29-21-10-4-3-9-20(21)27-16-14-26(15-17-27)13-7-6-12-25-24(28)23-18-19-8-2-5-11-22(19)30-23/h2-5,8-11,18H,6-7,12-17H2,1H3,(H,25,28) Isomere SMILES COC1=CC=CC=C1N2CCN(CC2)CCCCNC(=O)C3=CC4=CC=CC=C4S3 Molekulargewicht 423.57 Reaxy-Rn 9295580 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9295580&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 Organoheterocyclic compounds Klasse Diazinanes Subclass Piperazines Intermediate Tree Nodes Not available Direct Parent Phenylpiperazines Alternative Parents N-arylpiperazines Aminophenyl ethers Methoxyanilines 1-benzothiophenes Methoxybenzenes 2,3,5-trisubstituted thiophenes Dialkylarylamines Anisoles 2-heteroaryl carboxamides Phenoxy compounds Thiophene carboxamides N-alkylpiperazines Alkyl aryl ethers Heteroaromatic compounds Amino acids and derivatives Trialkylamines Secondary carboxylic acid amides Azacyclic compounds Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents N-arylpiperazine - Phenylpiperazine - Methoxyaniline - Aminophenyl ether - Benzothiophene - 1-benzothiophene - Thiophene carboxylic acid or derivatives - Thiophene carboxamide - Tertiary aliphatic/aromatic amine - 2-heteroaryl carboxamide - Anisole - Phenol ether - Phenoxy compound - Methoxybenzene - Aniline or substituted anilines - Dialkylarylamine - 2,3,5-trisubstituted thiophene - Alkyl aryl ether - N-alkylpiperazine - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Thiophene - Tertiary aliphatic amine - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Tertiary amine - Azacycle - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group. 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-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Empfindlichkeit Light sensitive Molekulargewicht 423.600 g/mol XLogP3 4.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 8 Exact Mass 423.198 Da Monoisotopic Mass 423.198 Da Topological Polar Surface Area 73.100 Ų Heavy Atom Count 30 Formal Charge 0 Complexity 541.000 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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