340162-93-8

Basic information

• Product Name: Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methyl-
• CAS NO: 340162-93-8
• Molecular Formula: C20H25N3O7
• Molecular Weight: 419.434
• Mol File: 340162-93-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methyl-(340162-93-8)
• EPA Substance Registry System: Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methyl-(340162-93-8)

Safety Data

• Hazardous Substances Data: 340162-93-8(Hazardous Substances Data)

Usage

Description

Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methylis a chemical compound with the molecular formula C26H29N3O8P. It is a modified form of cytidine, a nucleoside that is a building block of RNA. The N-benzoyl-2'-O-(2-methoxyethyl)-5-methylmodification of cytidine enhances its stability and potency, making it a potential candidate for use in pharmaceuticals and research.

Uses

Used in Pharmaceutical Industry:
Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methylis used as a modified nucleoside for the development of new drugs for various medical conditions. Its enhanced stability and potency make it a promising candidate for pharmaceutical applications.
Used in Research:
Cytidine, N-benzoyl-2'-O-(2-methoxyethyl)-5-methylis used as a research tool for studying RNA modifications and nucleoside analogues. Its unique properties and potential applications make it of interest to scientists in the field of RNA biology and drug development.
Further research is needed to fully understand the potential applications and biological effects of this modified cytidine compound.

Upstream product

• 182496-01-1 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-(2-methoxyethyl)-N₄-benzoyl-5-methylcytidine 
• 440327-53-7 N-benzoyl-3',5'-di-O-levulinyl-2'-O-(2-methoxyethyl)-5-methylcytidine 

Downstream Products

• 440327-53-7 N-benzoyl-3',5'-di-O-levulinyl-2'-O-(2-methoxyethyl)-5-methylcytidine 
• 182496-01-1 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-(2-methoxyethyl)-N₄-benzoyl-5-methylcytidine 

Relevant articles and documents

DDQ mediated regiospecific protection of primary alcohol and deprotection under neutral conditions: Application of new p-methoxy benzyl-pixyl ether as reagent of choice for nucleoside protection

A simple and efficient protocol is described for regiosepecific protection of primary hydroxyl group both in nucleosides and other molecules with p-methoxy-benzyl 2,7-dimethyl pixylether (MBDPE) in presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ). Furthermore, swift deprotection of 2, 7-dimethylpixyl (DMPx) is accomplished with DDQ in MeOH. Both procedures are successfully implemented on gram-scale synthesis of modified nucleosides. This protocol offers mild and neutral conditions for selective protection and deprotection of DMPx group while compatible in presence of other conventional protecting groups such as benzoyl, benzyl, THP, TBDPS and acetonide.

Renewable amberlyst-15 catalyzed highly regioselective tritylation and deprotection of sugar-based diols

Amberlyst-15 catalyzed highly regioselective tritylation of sugar-based diols was achieved under mild condition using 4,4′-dimethoxytrityl alcohol (DMTrOH). Deprotection of the corresponding DMTr group was also established by the variation to protic solvent. Meanwhile, the heterogeneous catalyst Amberlyst-15 was recycled 3 times with satisfactory retention of catalytic activity and proved its potential application in industry.