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 5-(Benzyloxy)indole - ≥98% , CAS No.1215-59-4
Synonyms
NSC 62895 | 5-(Benzyloxy)-1H-indole # | 5-Benzyloxyindole | BENZYL 1H-INDOL-5-YL ETHER | NSC62895 | NSC-62895 | WLN: T56 BMJ GO1R | 5-(Benzyloxy)indole, 95% | SY004490 | FT-0602806 | IDI1_018175 | BBL010818 | AM20060941 | Benzyloxy-5 indole [French] | F00
Storage
Store at 2-8°C,Protected from light,Argon charged
🧪
Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 1.Reactant in regio- and stereoselective morpholine-catalyzed direct C-3 alkenylation with α,β-unsaturated aldehydes.
2.Reactant in selective debenzylation of protective groups using SiliaCat-palladium under mild reaction conditions.
3.Reactant in metal-free Friedel-Crafts alkylation reactions.
4.Reactant in preparation of protein kinase (PKC) inhibitors.
5.Reactant in preparation of indole/quinoline carbothioic acid amide derivatives.
Specifications Synonyms
NSC 62895 | 5-(Benzyloxy)-1H-indole # | 5-Benzyloxyindole | BENZYL 1H-INDOL-5-YL ETHER | NSC62895 | NSC-62895 | WLN: T56 BMJ GO1R | 5-(Benzyloxy)indole, 95% | SY004490 | FT-0602806 | IDI1_018175 | BBL010818 | AM20060941 | Benzyloxy-5 indole [French] | F00
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Protected from light, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1=CC=C(C=C1)COC2=CC3=C(C=C2)NC=C3 IUPAC Name 5-phenylmethoxy-1H-indole InChIKey JCQLPDZCNSVBMS-UHFFFAOYSA-N INCHI 1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-6-7-15-13(10-14)8-9-16-15/h1-10,16H,11H2 Isomeric SMILES C1=CC=C(C=C1)COC2=CC3=C(C=C2)NC=C3 WGK Germany 3 RTECS NL4850000 UN Number 2811 Packing Group III Molecular Weight 223.27 Beilstein 173532 Reaxy-Rn 173532 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=173532&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 Indoles and derivatives Subclass Indoles Intermediate Tree Nodes Not available Direct Parent Indoles Alternative Parents Alkyl aryl ethers Benzene and substituted derivatives Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Azacycle - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen 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.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Air sensitive；Light sensitive Melt Point(°C) 96-101°C Molecular Weight 223.270 g/mol XLogP3 3.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 3 Exact Mass 223.1 Da Monoisotopic Mass 223.1 Da Topological Polar Surface Area 25.000 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 237.000 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.
H1408097