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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items N6-Benzyladenosine - ≥99% , CAS No.4294-16-0
Synonyms
AS-55043 | (2R,3R,4S,5R)-2-[6-(benzylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol | Q8C | 6-Benzylamino-9-(beta-D-ribofuranosyl)purine | C17H19N5O4 | SCHEMBL219438 | N6-benzylado | NSC 70423 | N(6)-Benzyladenosine | W12788 | Q27236958 | Discontinue
Storage
Argon charged,Room temperature
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Why this grade ≥99% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
AS-55043 | (2R, 3R, 4S, 5R)-2-[6-(benzylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3, 4-diol | Q8C | 6-Benzylamino-9-(beta-D-ribofuranosyl)purine | C17H19N5O4 | SCHEMBL219438 | N6-benzylado | NSC 70423 | N(6)-Benzyladenosine | W12788 | Q27236958 | Discontinue
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Nombres e identificadores Sonrisas canónicas C1=CC=C(C=C1)CNC2=C3C(=NC=N2)N(C=N3)C4C(C(C(O4)CO)O)O IUPAC Name (2R,3R,4S,5R)-2-[6-(benzylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol InChIKey MRPKNNSABYPGBF-LSCFUAHRSA-N INCHI 1S/C17H19N5O4/c23-7-11-13(24)14(25)17(26-11)22-9-21-12-15(19-8-20-16(12)22)18-6-10-4-2-1-3-5-10/h1-5,8-9,11,13-14,17,23-25H,6-7H2,(H,18,19,20)/t11-,13-,14-,17-/m1/s1 Isómeros SMILES C1=CC=C(C=C1)CNC2=C3C(=NC=N2)N(C=N3)[C@H]4[C@@H]([C@@H]([C@H](O4)CO)O)O WGK Alemania 3 Peso molecular 357.36 Beilstein 56815 Reaxy-Rn 1230574 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1230574&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 Nucleosides, nucleotides, and analogues Clase Purine nucleosides Subclass Not available Intermediate Tree Nodes Not available Direct Parent Purine nucleosides Alternative Parents 6-alkylaminopurines Glycosylamines Pentoses Benzylamines Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Benzenoid - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Tetrahydrofuran - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Secondary amine - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Amine - Organooxygen compound - Organopnictogen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad air sensitive Punto de fusión (°C) 184-186°C Peso molecular 357.400 g/mol XLogP3 1.100 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 5 Exact Mass 357.144 Da Monoisotopic Mass 357.144 Da Topological Polar Surface Area 126.000 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 466.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 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
Preguntas frecuentes y artículos Citations of This Product Referencias 1. Qiqi Quan, Zhiwei Liu, Zhaodong Li, Kangliang Pan, Anastasios Koidis, Yi Lei, Xiaoqin Yu, Qiuhua Mo, Xinan Huang, Hongtao Lei. (2023) Authenticating Emergent Adulterant 6-Benzylaminopurine in Bean Sprouts: Virtual Hapten Similarity Enhanced Immunoassay. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:37199564 ] [10.1021/acs.jafc.3c01696 ]
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