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Merck
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重要文件

410756

Sigma-Aldrich

(2-氧代-2-苯乙基)膦酸二乙酯

97%

同義詞:

Diethyl benzoylmethylphosphonate, Diethyl phenacylphosphonate, NSC 648426

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About This Item

線性公式:
C6H5COCH2P(O)(OC2H5)2
CAS號碼:
分子量::
256.23
MDL號碼:
分類程式碼代碼:
12352108
PubChem物質ID:
NACRES:
NA.22

化驗

97%

反應適用性

reaction type: C-C Bond Formation

折射率

n20/D 1.513 (lit.)

bp

192-193 °C/11 mmHg (lit.)

密度

1.179 g/mL at 25 °C (lit.)

官能基

ketone
phenyl
phosphonate

SMILES 字串

CCOP(=O)(CC(=O)c1ccccc1)OCC

InChI

1S/C12H17O4P/c1-3-15-17(14,16-4-2)10-12(13)11-8-6-5-7-9-11/h5-9H,3-4,10H2,1-2H3

InChI 密鑰

HPEVTTNSIPGLEL-UHFFFAOYSA-N

應用

Reactant involved in:
  • Asymmetric Michael addition of β-oxo phosphonates to nitro olefins
  • Gem-chlorofluorination of keto phosphonates with subsequent functionalization of the products
  • Cyclocondensation reactions to produce arylphosphonates
  • Diazo transfer reactions for synthesis of diazo-phosphonyl compounds
  • Horner-Wadsworth-Emmons reactions
  • Inverse-electron-demand Diels-Alder reactions

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


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分析證明 (COA)

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Douglass F Taber et al.
Tetrahedron letters, 49(48), 6904-6906 (2009-12-01)
An convenient reagent for the one-carbon homologation of an aldehyde to the corresponding alkyne is reported. This reagent allows this conversion to conveniently be carried out on a large scale under ambient conditions.

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