The store will not work correctly when cookies are disabled.
Javascript est désactivé dans votre navigateur. Pour une meilleure expérience sur notre site, assurez-vous d’activer JavaScript dans votre navigateur.
· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock PF9601N - ≥98% , CAS No.133845-63-3
Synonyms
AC-36581 | EX-A4722 | (5-Benzyloxy-1H-indol-2-ylmethyl)-prop-2-ynyl-amine | N-((5-(benzyloxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine | N-[(5-phenylmethoxy-1H-indol-2-yl)methyl]prop-2-yn-1-amine | AKOS037643452 | HY-120419 | F90321 | PF9601N | PF-9601N | A
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.
Vue d’ensemble Information
PF9601N is a potent and selective inhibitor of monoamine oxidase B that exhibits anti-Parkinsonian effects in several models of PD.
Specifications Synonymes
AC-36581 | EX-A4722 | (5-Benzyloxy-1H-indol-2-ylmethyl)-prop-2-ynyl-amine | N-((5-(benzyloxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine | N-[(5-phenylmethoxy-1H-indol-2-yl)methyl]prop-2-yn-1-amine | AKOS037643452 | HY-120419 | F90321 | PF9601N | PF-9601N | A
Spécifications et pureté
≥98%
Mécanismes biochimiques et physiologiques
PF9601N is a potent and selective inhibitor of monoamine oxidase B that exhibits anti-Parkinsonian effects in several models of PD.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Pubchem Sid 528766626 Sourires canoniques C#CCNCC1=CC2=C(N1)C=CC(=C2)OCC3=CC=CC=C3 IUPAC Name N-[(5-phenylmethoxy-1H-indol-2-yl)methyl]prop-2-yn-1-amine InChIKey YFPNAYXYKXAKJC-UHFFFAOYSA-N INCHI 1S/C19H18N2O/c1-2-10-20-13-17-11-16-12-18(8-9-19(16)21-17)22-14-15-6-4-3-5-7-15/h1,3-9,11-12,20-21H,10,13-14H2 Isomères SMILES C#CCNCC1=CC2=C(N1)C=CC(=C2)OCC3=CC=CC=C3 WGK Allemagne 3 PubChem CID 9947954 Poids moléculaire 290.36
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 Classe Indoles and derivatives Subclass Indoles Intermediate Tree Nodes Not available Direct Parent Indoles Alternative Parents Aralkylamines Alkyl aryl ethers Substituted pyrroles Benzene and substituted derivatives Heteroaromatic compounds Dialkylamines Azacyclic compounds Acetylides Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Secondary aliphatic amine - Ether - Acetylide - Secondary amine - Azacycle - Organonitrogen compound - Organopnictogen compound - Amine - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 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.
Structure 3D Cibles associées (humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 290.400 g/mol XLogP3 3.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 6 Exact Mass 290.142 Da Monoisotopic Mass 290.142 Da Topological Polar Surface Area 37.100 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 382.000 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
Calculateurs de solution 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 Avis
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. Paramètres Accepter tout Refuser
Shall we send you a message when we have discounts available?
Remind me later Autoriser
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.
B2402482