256224-13-2

Basic information

• Product Name: 2-AMINO-2'-O-(2-METHOXYETHYL)ADENOSINE
• Synonyms: 2-AMINO-2'-O-(2-METHOXYETHYL)ADENOSINE;2'-O-(2-Methoxyethyl)-2-aminoadenosine
• CAS NO: 256224-13-2
• Molecular Formula: C₁₃H₂₀N₆O₅
• Molecular Weight: 340.34
• Mol File: 256224-13-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-AMINO-2'-O-(2-METHOXYETHYL)ADENOSINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-2'-O-(2-METHOXYETHYL)ADENOSINE(256224-13-2)
• EPA Substance Registry System: 2-AMINO-2'-O-(2-METHOXYETHYL)ADENOSINE(256224-13-2)

Safety Data

• Hazardous Substances Data: 256224-13-2(Hazardous Substances Data)

Usage

General Description

2-Amino-2'-O-(2-methoxyethyl)adenosine is a chemical compound that belongs to the class of adenosine derivatives. It is a modified form of adenosine, where the hydroxyl group at the 2' position is substituted with a 2-methoxyethyl group. This modification enhances the compound's stability and can potentially alter its biological activity. Adenosine derivatives, including 2-amino-2'-O-(2-methoxyethyl)adenosine, are known for their role in various physiological processes, including neurotransmission, energy metabolism, and immune response. These compounds have been studied for their potential therapeutic applications, particularly in the treatment of neurological and cardiovascular disorders.

Upstream product

• 6482-24-2 2-Bromoethyl methyl ether 
• 2096-10-8 adenosine-2-amine 
• 16427-44-4 2-methoxyethyl methanesulfonate 
• 17178-10-8 2-methoxy-ethyl p-toluenesulfonyloxy ester 

Downstream Products

• 251647-50-4 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-(2-methoxyethyl)-N²-isobutyrylguanosine 

Relevant articles and documents

An improved process for the manufacture of 5′-O-(4,4′-dimethoxytrityl)-N2-isobutyryl-2′-O-(2-methoxyethyl)guanosine

A revised, optimized process for the manufacture of 5′-O-(4,4′-dimethoxytrityl)-N2-isobutyryl-2′-O-(2- methoxyethyl)guanosine (MOE G PNS) that controls critical impurities to less than 0.2% was developed. The 2′-O-alkylation of 2,6-diaminopurine riboside

2'-O-MOE-3'-H-phosphorothioate nucleoside monomer and synthetic method thereof

The invention discloses 2'-O-MOE-3'-H-phosphorodithioate ribonucleotide and 2'-O-MOE-3'-H-phosphorothioate ribonucleotide and precursor compounds thereof, preparation methods and applications of the 2'-O-MOE-3'-H-phosphorodithioate ribonucleotide and the

Synthesis study of 2′-O-(2-methoxyethyl)-purine derivatives

Alkylation of adenosine and 2-aminoadenosine was studied in dimethylsulfoxide with application of 1-methanesulfonyloxy-2-methoxyethane as an alkylating agent and t-BuOK, KOH and NaH as bases under mild heating. Using new reaction conditions, the improved synthesis of 2′-O-MOE-purine derivatives is described. Copyright Taylor & Francis Group, LLC.