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Usage

Chemical class

Amino alcohols
A class of organic compounds containing both an amino group (-NH2) and a hydroxyl group (-OH) attached to a carbon chain.

6-chloropurin-9-ylphenyl group

A derivative of purine, a heterocyclic aromatic organic compound found in DNA and RNA, with a chlorine atom attached at the 6-position and a phenyl group at the 9-position.

2-hydroxyethylamino group

An amino group (-NH2) attached to an ethyl chain, with a hydroxyl group (-OH) attached to the second carbon of the chain.

Ethanol group

A two-carbon chain with a hydroxyl group (-OH) attached to each carbon.

Potential use as a therapeutic agent

The presence of the 2-hydroxyethylamino group makes 2-[[4-(6-chloropurin-9-yl)phenyl]-(2-hydroxyethyl)amino]ethanol a candidate for various therapeutic applications, as it may interact with biological targets in the body.

May be used in drug development

Due to its unique structure and potential interactions with biological targets, 2-[[4-(6-chloropurin-9-yl)phenyl]-(2-hydroxyethyl)amino]ethanol can be used as a research tool to study the effects of similar compounds and their potential as therapeutic agents.

A chemically complex compound

The presence of multiple functional groups and its structure make 2-[[4-(6-chloropurin-9-yl)phenyl]-(2-hydroxyethyl)amino]ethanol a complex molecule with a variety of potential interactions and applications.

In the pharmaceutical industry

Due to its potential therapeutic applications and its ability to serve as a research tool, 2-[[4-(6-chloropurin-9-yl)phenyl]-(2-hydroxyethyl)amino]ethanol may have a significant impact on drug development and the understanding of biological processes.

In biochemical research

The compound's structure and potential interactions with biological targets make it a valuable tool for studying various biochemical processes and the development of new therapeutic agents.