The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
· · COA & SDS available for every product · Same-day shipping on in-stock items Farampator - ≥98% , Glutamate receptor ionotropic AMPA positive allosteric modulator, CAS No.211735-76-1, Glutamate receptor ionotropic AMPA positive allosteric modulator
Synonyms
Piperidine, 1-(2,1,3-benzoxadiazol-5-ylcarbonyl)- | Q5434818 | 7X6P5N8K2L | Org24448 | Org-24448 | BCP28990 | A935040 | AC-36657 | CX691;1-(benzofurazan-5-ylcarbonyl)piperidine | CX-691;Org24448 | EX-A4789 | 2,1,3-benzoxadiazol-5-yl(piperidin-1-yl)methano
Shipped In
Ice chest + Ice pads
🧪
Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
📋
Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Information
Farampator (CX691, Org24448) is a positive modulator of AMPA receptor.
Specifications Synonyms
Piperidine, 1-(2, 1, 3-benzoxadiazol-5-ylcarbonyl)- | Q5434818 | 7X6P5N8K2L | Org24448 | Org-24448 | BCP28990 | A935040 | AC-36657 | CX691;1-(benzofurazan-5-ylcarbonyl)piperidine | CX-691;Org24448 | EX-A4789 | 2, 1, 3-benzoxadiazol-5-yl(piperidin-1-yl)methano
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Farampator (CX691, Org24448) is a positive modulator of AMPA receptor.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
POSITIVE ALLOSTERIC MODULATOR
Mechanism of action
Glutamate receptor ionotropic AMPA positive allosteric modulator
Product Properties Names and Identifiers Pubchem Sid 504762853 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762853 Canonical Smiles C1CCN(CC1)C(=O)C2=CC3=NON=C3C=C2 IUPAC Name 2,1,3-benzoxadiazol-5-yl(piperidin-1-yl)methanone InChIKey XFVRBYKKGGDPAJ-UHFFFAOYSA-N INCHI 1S/C12H13N3O2/c16-12(15-6-2-1-3-7-15)9-4-5-10-11(8-9)14-17-13-10/h4-5,8H,1-3,6-7H2 Isomeric SMILES C1CCN(CC1)C(=O)C2=CC3=NON=C3C=C2 Molecular Weight 231.25 Reaxy-Rn 13677286 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13677286&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 Class Piperidines Subclass N-acylpiperidines Intermediate Tree Nodes Not available Direct Parent N-benzoylpiperidines Alternative Parents Benzoxadiazoles Benzenoids Tertiary carboxylic acid amides Heteroaromatic compounds Furazans Oxacyclic compounds Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents N-benzoylpiperidine - Benzoxadiazole - Benzenoid - Azole - Furazan - Heteroaromatic compound - Oxadiazole - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Oxacycle - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as n-benzoylpiperidines. These are heterocyclic Compounds containing a piperidine ring conjugated to a benzyl group through one nitrogen ring atom. 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) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 231.250 g/mol XLogP3 1.500 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 231.101 Da Monoisotopic Mass 231.101 Da Topological Polar Surface Area 59.200 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 291.000 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
Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Settings Agree All Decline
Shall we send you a message when we have discounts available?
Remind me later Allow
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
B2313362