Diethyl (2-oxo-2-phenylethyl)phosphonate

• Catalog No.: 410756
• CAS Number: 3453-00-7
• M. F.: C12H17O4P
• M. W.: 256.234741
• Purity: 97%

SYNONYMS

• Title: (2-氧代-2-苯乙基)膦酸二乙酯
• IUPAC name: diethyl (2-oxo-2-phenylethyl)phosphonate
• IUPAC Traditional name: diethyl 2-oxo-2-phenylethylphosphonate
• Synonyms: NSC 648426; Diethyl phenacylphosphonate; Diethyl benzoylmethylphosphonate

DATABASE IDS

• CAS Number: 3453-00-7
• PubChem SID: 24865704
• MDL Number: MFCD00015342

PROPERTIES

• Linear Formula: C6H5COCH2P(O)(OC2H5)2
• Purity: 97%
• Boiling Point: 192-193 °C/11 mmHg(lit.)
• Density: 1.179 g/mL at 25 °C(lit.)
• Flash Point: >113 °C
• Flash Point: >235.4 °F
• Refractive Index: n20/D 1.513(lit.)
• Personal Protective Equipment: Eyeshields, Gloves
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Asymmetric Michael addition of β-oxo phosphonates to nitro olefins1
• Gem-chlorofluorination of keto phosphonates with subsequent functionalization of the products2
• Cyclocondensation reactions to produce arylphosphonates3
• Diazo transfer reactions for synthesis of diazo-phosphonyl compounds4
• Horner-Wadsworth-Emmons reactions5
• Inverse-electron-demand Diels-Alder reactions6

Description (简体中文)

包装
1, 10 g in glass bottle
Application
Reactant involved in:
• Asymmetric Michael addition of β-oxo phosphonates to nitro olefins1
• Gem-chlorofluorination of keto phosphonates with subsequent functionalization of the products2
• Cyclocondensation reactions to produce arylphosphonates3
• Diazo transfer reactions for synthesis of diazo-phosphonyl compounds4
• Horner-Wadsworth-Emmons reactions5
• Inverse-electron-demand Diels-Alder reactions6