CAS:
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone
Properties:
- Product Name: [3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone]
- Synonyms: null
- CAS: null
- EINECS: null
- Molecular Weight: null
- Molecular Formula: null
- Density: null
- Boiling Point(℃): null
- Flash Point(℃): null
- Refractive Index: null
- Hazard Symbols: null
- Risk Codes: null
- Safety Description: null
FAQ:
What is the chemical structure of
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid,
γ-lactone?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone is a compound with the chemical formula C14H11FO5. It is a lactone derivative of a pentonic acid, containing a fluorine atom and a methyl group.
What are the potential applications of 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone has potential applications in medicinal chemistry, as a building block for the synthesis of complex molecules, and in biochemical research as a tool for studying specific biological processes.
How is 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone synthesized?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone can be synthesized through a multistep chemical reaction starting from commercially available starting materials. The specific synthesis route may vary depending on the desired enantiomeric purity and overall yield of the compound.
What are the key characteristics of 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone that make it suitable for various applications?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone offers a unique combination of structural features, including a fluorine atom and a methyl group, that can impart specific chemical reactivity and biological activity to the compound. Its lactone structure also makes it amenable to ring-opening reactions for further functionalization.
What are the safety considerations for handling and using 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone in a laboratory setting?
As with any chemical compound, proper safety precautions should be followed when handling and using 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone in a laboratory setting. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following established protocols for handling and disposal of the compound.
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone is a compound with the chemical formula C14H11FO5. It is a lactone derivative of a pentonic acid, containing a fluorine atom and a methyl group.
What are the potential applications of 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone has potential applications in medicinal chemistry, as a building block for the synthesis of complex molecules, and in biochemical research as a tool for studying specific biological processes.
How is 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone synthesized?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone can be synthesized through a multistep chemical reaction starting from commercially available starting materials. The specific synthesis route may vary depending on the desired enantiomeric purity and overall yield of the compound.
What are the key characteristics of 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone that make it suitable for various applications?
3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone offers a unique combination of structural features, including a fluorine atom and a methyl group, that can impart specific chemical reactivity and biological activity to the compound. Its lactone structure also makes it amenable to ring-opening reactions for further functionalization.
What are the safety considerations for handling and using 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone in a laboratory setting?
As with any chemical compound, proper safety precautions should be followed when handling and using 3,5-dibenzoate-(2R)-2-deoxy-2-fluoro-2-methyl-D-erythro-Pentonic acid, γ-lactone in a laboratory setting. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following established protocols for handling and disposal of the compound.
