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· · COA & SDS available for every product · Same-day shipping on in-stock items 2'-O-MOE-5-Me-rU - ≥97% , CAS No.163759-49-7
Synonyms
SCHEMBL14824474 | Uridine, 2'-O-(2-methoxyethyl)-5-methyl- | 2'--O--Methoxyethyl-5-methyluridine | 2'--O-Methoxyethyl-5-methyluridine | 2'-o-methoxyethyl-5-methyluridine | 2'O-Methoxyethyl-5-methyluridine | 9Q36I4D9VB | J-700309 | AC-24669 | MFCD02682964
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 2'-O-MOE-5-Me-rU is an active compound. 2'-O-MOE-5-Me-rU can be used for oligonucleotide synthesis.
Form:Solid
Specifications Synonyms
SCHEMBL14824474 | Uridine, 2'-O-(2-methoxyethyl)-5-methyl- | 2'--O--Methoxyethyl-5-methyluridine | 2'--O-Methoxyethyl-5-methyluridine | 2'-o-methoxyethyl-5-methyluridine | 2'O-Methoxyethyl-5-methyluridine | 9Q36I4D9VB | J-700309 | AC-24669 | MFCD02682964
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
2'-O-MOE-5-Me-rU is an active compound . 2'-O-MOE-5-Me-rU can be used for oligonucleotide synthesis.
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 CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)OCCOC IUPAC Name 1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)oxolan-2-yl]-5-methylpyrimidine-2,4-dione InChIKey NEVQCHBUJFYGQO-DNRKLUKYSA-N INCHI 1S/C13H20N2O7/c1-7-5-15(13(19)14-11(7)18)12-10(21-4-3-20-2)9(17)8(6-16)22-12/h5,8-10,12,16-17H,3-4,6H2,1-2H3,(H,14,18,19)/t8-,9-,10-,12-/m1/s1 Isomeric SMILES CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)OCCOC Molecular Weight 316.31
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 Class Pyrimidine nucleosides Subclass Not available Intermediate Tree Nodes Not available Direct Parent Pyrimidine nucleosides Alternative Parents Glycosylamines Pyrimidones Monosaccharides Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Secondary alcohols Lactams Azacyclic compounds Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Urea - Azacycle - Oxacycle - Ether - Organoheterocyclic compound - Dialkyl ether - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Alcohol - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine 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.
3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Air sensitive; Light sensitive Melt Point(°C) 122 °C Molecular Weight 316.310 g/mol XLogP3 -1.800 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 6 Exact Mass 316.127 Da Monoisotopic Mass 316.127 Da Topological Polar Surface Area 118.000 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 467.000 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
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