DMT-MOE-5-Me-Bz-rC - for DNA synthesis, Suitable for molecular biology, ≥98% , CAS No.182496-01-1

CAS: 182496-01-1 Cat. No.: D777120 Molecular Weight: 721.79 EC Number: 805-197-4

GRADE & PURITY Suitable for molecular biology, for DNA synthesis, ≥98%

Storage

Protected from light,Room temperature

Shipped In

Normal

Overview

The product can be used for nucleic acid synthesis: as a modified cytidine, it is mainly used for nucleic acid synthesis, especially as an intermediate for synthesizing modified oligonucleotides.

Specifications

Specifications & Purity

for DNA synthesis, Suitable for molecular biology, ≥98%

Storage

Protected from light, Room temperature

Shipped In

Normal

Grade

for DNA synthesis, Suitable for molecular biology

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CC1=CN(C(=O)N=C1NC(=O)C2=CC=CC=C2)C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O)OCCOC
• IUPAC Name: N-[1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxy-3-(2-methoxyethoxy)oxolan-2-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide
• InChIKey: BYSCLUAIKFEFAH-LZURGKRNSA-N
• INCHI: 1S/C41H43N3O9/c1-27-25-44(40(47)43-37(27)42-38(46)28-11-7-5-8-12-28)39-36(51-24-23-48-2)35(45)34(53-39)26-52-41(29-13-9-6-10-14-29,30-15-19-32(49-3)20-16-30)31-17-21-33(50-4)22-18-31/h5-22,25,34-36,39,45H,23-24,26H2,1-4H3,(H,42,43,46,47)/t34-,35-,36-,39-/m1/s1
• Isomeric SMILES: CC1=CN(C(=O)N=C1NC(=O)C2=CC=CC=C2)[C@H]3[C@@H]([C@@H]([C@H](O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O)OCCOC
• Alternate CAS: 182496-01-1
• Molecular Weight: 721.79

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 Benzamides Benzylethers Anisoles Phenoxy compounds Benzoyl derivatives Methoxybenzenes Alkyl aryl ethers Pyrimidones Hydropyrimidines Imidolactams Monosaccharides Heteroaromatic compounds Oxolanes Secondary carboxylic acid amides Secondary alcohols Dialkyl ethers Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Triphenyl compound - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Benzamide - Benzoic acid or derivatives - Benzylether - Phenol ether - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Monosaccharide - Pyrimidine - Monocyclic benzene moiety - Hydropyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Organooxygen compound - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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