DMT-MOE-iBu-rG - for DNA synthesis, Suitable for molecular biology, ≥98% , CAS No.251647-50-4

CAS: 251647-50-4 Cat. No.: A777119 Formula: C₃₈H₄₃N₅O₉ Peso molecolare: 713.77

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

Storage

Protected from light,Room temperature

Shipped In

Normal

Panoramica

The compound is mainly used for nucleic acid synthesis, especially as an intermediate for synthesizing modified oligonucleotides. The protective groups (such as dimethoxytriphenylmethyl, DMT) and modifying groups (such as 2'-O- methoxyethyl, MOE) in its structure make it have specific chemical stability and biological activity in the synthesis process.

Specifications

Specifiche e purezza

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

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature

Spedito in

Normal

Grado

for DNA synthesis, Suitable for molecular biology

Purezza

≥98%

Nomi e identificatori

Sorrisi canonici

CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2C3C(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-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxy-3-(2-methoxyethoxy)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide

InChIKey

XDLPRZLZAFJSMA-BEGXHNNXSA-N

INCHI

1S/C38H43N5O9/c1-23(2)34(45)41-37-40-33-30(35(46)42-37)39-22-43(33)36-32(50-20-19-47-3)31(44)29(52-36)21-51-38(24-9-7-6-8-10-24,25-11-15-27(48-4)16-12-25)26-13-17-28(49-5)18-14-26/h6-18,22-23,29,31-32,36,44H,19-21H2,1-5H3,(H2,40,41,42,45,46)/t29-,31-,32-,36-/m1/s1

Isomeri SMILES

CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2[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

Peso molecolare

713.77

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Triphenyl compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenyl compounds
• Alternative Parents: Purine nucleosides Glycosylamines 6-oxopurines Hypoxanthines Benzylethers Anisoles Phenoxy compounds Methoxybenzenes N-arylamides Alkyl aryl ethers Pyrimidones N-substituted imidazoles Monosaccharides Vinylogous amides Oxolanes Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Dialkyl ethers Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Triphenyl compound - Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-oxopurine - Hypoxanthine - Benzylether - Purine - Imidazopyrimidine - Phenoxy compound - Methoxybenzene - N-arylamide - Phenol ether - Anisole - Alkyl aryl ether - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Oxacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Alcohol - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Aromatic heteropolycyclic compound
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Sensitive to light