DMT-rU - BioReagent, Biosynthesis, Suitable for molecular biology, ≥98% , CAS No.81246-79-9

CAS: 81246-79-9 Cat. No.: D777111 Molecular Weight: 546.58

GRADE & PURITY Suitable for molecular biology, BioReagent, Biosynthesis, ≥98%

Synonyms

5'-O-DMT-rU

Storage

Protected from light,Room temperature

Shipped In

Normal

Overview

5'-O-DMT-rU is a modified nucleoside and can be used to synthesize RNA.

Specifications

Synonyms

5'-O-DMT-rU

Specifications & Purity

BioReagent, Biosynthesis, Suitable for molecular biology, ≥98%

Storage

Protected from light, Room temperature

Shipped In

Normal

Grade

BioReagent, Biosynthesis, Suitable for molecular biology

Purity

≥98%

Names and Identifiers

• Canonical Smiles: COC1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=C(C=C3)OC)OCC4C(C(C(O4)N5C=CC(=O)NC5=O)O)O
• IUPAC Name: 1-[(2R,3R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione
• InChIKey: PCFSNQYXXACUHM-YULOIDQLSA-N
• INCHI: 1S/C30H30N2O8/c1-37-22-12-8-20(9-13-22)30(19-6-4-3-5-7-19,21-10-14-23(38-2)15-11-21)39-18-24-26(34)27(35)28(40-24)32-17-16-25(33)31-29(32)36/h3-17,24,26-28,34-35H,18H2,1-2H3,(H,31,33,36)/t24-,26-,27-,28-/m1/s1
• Isomeric SMILES: COC1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=C(C=C3)OC)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CC(=O)NC5=O)O)O
• Molecular Weight: 546.58

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Triphenyl compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenyl compounds
• Alternative Parents: Pyrimidine nucleosides Glycosylamines Pentoses Benzylethers Anisoles Methoxybenzenes Phenoxy compounds Pyrimidones Alkyl aryl ethers Hydropyrimidines Oxolanes Heteroaromatic compounds Vinylogous amides 1,2-diols Secondary alcohols Lactams Ureas Oxacyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Triphenyl compound - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzylether - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Hydropyrimidine - Monosaccharide - Monocyclic benzene moiety - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Lactam - 1,2-diol - Secondary alcohol - Urea - Oxacycle - Azacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Organic oxide - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Sensitive to light