DMT-OMe-Ac-rC - for DNA synthesis, Suitable for molecular biology, ≥98% , CAS No.199593-08-3

CAS: 199593-08-3 Cat. No.: D777113 Molecular Weight: 601.66

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

Synonyms

5'-O-DMT-N4-Acetyl-2'-O-Methyl-cytidine | N-(1-((2R,3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide | N4-Acetyl-2'-deoxy-2'-fluorocytidine | 5'-DMT-2'-OMe-Ac-C | N4-Ac-DMT-2'-OMe-Cr | N4-acetyl

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

DMT-ome-RC (AC) (n-acetyl-5'-o-(4,4'-dimethyltrityl)-2'-o-methylcytidine) is a nucleotide derivative, which can be used to synthesize oligoribonucleotides.

Specifications

Synonyms

5'-O-DMT-N4-Acetyl-2'-O-Methyl-cytidine | N-(1-((2R, 3R, 4R, 5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1, 2-dihydropyrimidin-4-yl)acetamide | N4-Acetyl-2'-deoxy-2'-fluorocytidine | 5'-DMT-2'-OMe-Ac-C | N4-Ac-DMT-2'-OMe-Cr | N4-acetyl

Specifications & Purity

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

Stability And Storage

Store at room temperature (24 months).

Storage

Room temperature, Argon charged

Shipped In

Normal

Grade

for DNA synthesis, Suitable for molecular biology

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CC(=O)NC1=NC(=O)N(C=C1)C2C(C(C(O2)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)O)OC
• IUPAC Name: N-[1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxy-3-methoxyoxolan-2-yl]-2-oxopyrimidin-4-yl]acetamide
• InChIKey: FINUHOJILDNELQ-PMFUCWTESA-N
• INCHI: 1S/C33H35N3O8/c1-21(37)34-28-18-19-36(32(39)35-28)31-30(42-4)29(38)27(44-31)20-43-33(22-8-6-5-7-9-22,23-10-14-25(40-2)15-11-23)24-12-16-26(41-3)17-13-24/h5-19,27,29-31,38H,20H2,1-4H3,(H,34,35,37,39)/t27-,29-,30-,31-/m1/s1
• Isomeric SMILES: CC(=O)NC1=NC(=O)N(C=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)O)OC
• Molecular Weight: 601.66

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