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Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate (DMP) is a synthetic phosphonate ester that is widely used in scientific research. It has a variety of applications in biochemistry, organic chemistry, and biotechnology due to its unique properties. DMP is a versatile compound that can be used as a reagent, catalyst, or i...
Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate (DMP) is a synthetic phosphonate ester that is widely used in scientific research. It has a variety of applications in biochemistry, organic chemistry, and biotechnology due to its unique properties. DMP is a versatile compound that can be used as a reagent, catalyst, or inhibitor in a variety of reactions. It is also used as a substrate for enzymatic reactions and as a metabolic intermediate in biochemical pathways.
A significant application of phosphonate derivatives, including compounds similar to Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate, is in the synthesis of novel polymers. Yamabe et al. (2000) developed a method for synthesizing perfluorocarbon polymers with phosphono groups through copolymerization or terpolymerization processes. These polymers exhibit unique properties due to the incorporation of phosphono groups, highlighting their potential in advanced material applications (Yamabe, Akiyama, Akatsuka, & Kato, 2000).
Phosphonate derivatives are pivotal in organic synthesis, offering routes to regioselective syntheses of complex molecules. Watanabe, Ijichi, and Furukawa (1993) demonstrated a regioselective synthesis of dimethyl phthalide-3-phosphonates, showcasing the versatility of phosphonate derivatives in synthesizing compounds with various substituents on the benzene ring, which could be critical in developing pharmaceuticals and agrochemicals (Watanabe, Ijichi, & Furukawa, 1993).
In material sciences, the manipulation of phosphonate derivatives leads to the development of materials with specific functionalities. Higo and Kamata (1987) explored the surface reactions of dialkyl phosphite on alumina and magnesia, revealing the potential of phosphonate derivatives in modifying surface properties for various applications, including catalysis and material coatings (Higo & Kamata, 1987).
Feng, Ai, Cao, and Yang (2008) investigated Dimethyl methyl phosphonate (DMMP) as a non-flammable solvent for lithium batteries, demonstrating its potential to enhance safety and performance. Although DMMP differs from Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate, this research illustrates the broader applicability of phosphonate derivatives in developing advanced battery technologies (Feng, Ai, Cao, & Yang, 2008).
Product Name : | Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate | ||
CAS No. : | 50889-46-8 | Molecular Weight : | 258.20 |
MDL No. : | MFCD11707108 | Purity/ Specification : | |
Molecular Formula : | C9H17F2O4P | Storage : | Inert atmosphere,Room Temperature |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Warning | Precautionary Statements : | P261-P280-P305+P351+P338 |
UN# : | N/A | Class : | N/A |
Hazard Statements : | H302-H315-H319-H332-H335 | Packing Group : | N/A |