123919-20-0

Basic information

• Product Name: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methyl-
• Synonyms: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methyl-
• CAS NO: 123919-20-0
• Molecular Formula: C15H26O4
• Molecular Weight: 270.37
• Mol File: 123919-20-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methyl-(123919-20-0)
• EPA Substance Registry System: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methyl-(123919-20-0)

Safety Data

• Hazardous Substances Data: 123919-20-0(Hazardous Substances Data)

Usage

Description

.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylis a synthetic carbohydrate compound derived from ribose, a naturally occurring sugar. It features a complex molecular structure with a six-membered ring of carbon atoms and various functional groups, including an anhydro, cyclohexyl, ethyl, and methyl groups. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylhas potential applications in organic chemistry, biochemistry, and medicinal chemistry, making it a valuable tool for researchers studying carbohydrate chemistry and developing new therapeutic agents.

Uses

Used in Organic Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylis used as a synthetic building block for the development of complex organic molecules. Its unique structure allows for various chemical reactions and modifications, contributing to the synthesis of novel compounds with potential applications in different industries.
Used in Biochemistry:
In the field of biochemistry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylserves as a valuable research tool for studying the interactions between carbohydrates and other biomolecules. Its unique structure enables researchers to investigate the role of carbohydrates in biological processes and their potential as therapeutic targets.
Used in Medicinal Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylis used as a starting material for the development of new therapeutic agents. Its unique structure and properties make it an attractive candidate for the design and synthesis of novel drugs targeting various diseases, including cancer, infectious diseases, and metabolic disorders.
Used in Drug Delivery Systems:
In the pharmaceutical industry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylcan be employed as a component in the design of drug delivery systems. Its unique structure and functional groups can be utilized to improve the solubility, stability, and bioavailability of therapeutic agents, enhancing their efficacy and safety.
Used in Glycobiology Research:
In the field of glycobiology, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(1-cyclohexylethyl)-3-deoxy-2-O-methylis used as a model compound to study the role of carbohydrates in cell recognition, adhesion, and signaling. Its unique structure allows researchers to investigate the molecular mechanisms underlying these processes and develop new strategies for modulating carbohydrate-mediated interactions in various biological systems.