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

CAS: 81246-79-9 Cat. No.: D777111 Peso molecular: 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

Descripción general

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

Specifications

Sinónimos

5'-O-DMT-rU

Especificaciones y pureza

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

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Grado

BioReagent, Biosynthesis, Suitable for molecular biology

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: 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
• Isómeros 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
• Peso molecular: 546.58

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: 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
• Descripción: 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

Propiedades químicas y físicas

• Sensibilidad: Sensitive to light