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· · COA & SDS available for every product · Same-day shipping on in-stock items Ralfinamide (FCE-26742A) - Moligand™,≥95% , Glutamate [NMDA] receptor antagonist, CAS No.133865-88-0, Glutamate [NMDA] receptor antagonist
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥95% Synonyms
NW1029 | NW-1029 | DB06649 | 2-(((4-((2-fluorophenyl)methoxy)phenyl)methyl)amino)propanamide | DTXSID70158406 | NCGC00370789-01 | PNU-0154339E | MFCD08272558 | UNII-3LPF0S0GVV | (S)-2-[4-(2-fluorobenzyloxy)benzylamino]propanamide | DS-18607 | F12108 | FCE
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™,≥95% Moligand™ 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
NW1029 | NW-1029 | DB06649 | 2-(((4-((2-fluorophenyl)methoxy)phenyl)methyl)amino)propanamide | DTXSID70158406 | NCGC00370789-01 | PNU-0154339E | MFCD08272558 | UNII-3LPF0S0GVV | (S)-2-[4-(2-fluorobenzyloxy)benzylamino]propanamide | DS-18607 | F12108 | FCE
Specifications & Purity
Moligand™, ≥95%
Biochemical and Physiological Mechanisms
Ralfinamide (FCE-26742A) is a available Na+ blocker derived from α-aminoamide, with function of suppressing pain.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Glutamate [NMDA] receptor antagonist
Product Properties Names and Identifiers Canonical Smiles CC(C(=O)N)NCC1=CC=C(C=C1)OCC2=CC=CC=C2F IUPAC Name (2S)-2-[[4-[(2-fluorophenyl)methoxy]phenyl]methylamino]propanamide InChIKey BHJIBOFHEFDSAU-LBPRGKRZSA-N INCHI 1S/C17H19FN2O2/c1-12(17(19)21)20-10-13-6-8-15(9-7-13)22-11-14-4-2-3-5-16(14)18/h2-9,12,20H,10-11H2,1H3,(H2,19,21)/t12-/m0/s1 Isomeric SMILES C[C@@H](C(=O)N)NCC1=CC=C(C=C1)OCC2=CC=CC=C2F PubChem CID 5745207 Molecular Weight 302.34
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 amides Alternative Parents Alanine and derivatives Phenylmethylamines Phenoxy compounds Phenol ethers Benzylamines Fluorobenzenes Aralkylamines Alkyl aryl ethers Aryl fluorides Primary carboxylic acid amides Dialkylamines Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Alpha-amino acid amide - Alanine or derivatives - Phenoxy compound - Benzylamine - Phenol ether - Phenylmethylamine - Alkyl aryl ether - Fluorobenzene - Aralkylamine - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Primary carboxylic acid amide - Ether - Secondary aliphatic amine - Secondary amine - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide 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 Molecular Weight 302.340 g/mol XLogP3 2.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 7 Exact Mass 302.143 Da Monoisotopic Mass 302.143 Da Topological Polar Surface Area 64.400 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 346.000 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
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