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· · COA & SDS available for every product · Same-day shipping on in-stock items 5-(Benzyloxy)indole - ≥98%(with less than 4% ethanol) , 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
Argon charged,Room temperature
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Why this grade ≥98%(with less than 4% ethanol) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,Room temperature Ships Normal 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.
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%(with less than 4% ethanol)
Storage
Argon charged, Room temperature
Purity
≥98%(with less than 4% ethanol)
Names and Identifiers Pubchem Sid 488182011 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182011 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
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