Pharmaceutical

Dimethyl acetylmethylphosphonate

  • CAS: 4202-14-6
  • Purity: 99%
  • Factory Supply industrial standard Dimethyl acetylmethylphosphonate 4202-14-6 In Stock
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1.What is the Dimethyl acetylmethylphosphonate ?

Reagent used together with tosyl azide in a one-pot alkynylation of aldehydes.

chloroacetone
78-95-5

chloroacetone

phosphorous acid trimethyl ester
121-45-9

phosphorous acid trimethyl ester

dimethyl (2-oxopropyl)phosphonate
4202-14-6

dimethyl (2-oxopropyl)phosphonate

Conditions
Conditions Yield
In toluene; at 135 ℃; for 0.333333h; under 3750.38 - 15001.5 Torr; Large scale;
88%
chloroacetone; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 2h;
phosphorous acid trimethyl ester; In acetone; acetonitrile; at 50 ℃; for 24h;
82%
chloroacetone; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 2h; Irradiation;
phosphorous acid trimethyl ester; In acetone; acetonitrile; at 50 ℃; for 24h;
77%
chloroacetone; phosphorous acid trimethyl ester; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 1h; Inert atmosphere;
phosphorous acid trimethyl ester; at 20 - 50 ℃; for 12h; Inert atmosphere;
72%
With potassium iodide; In acetone; acetonitrile; at 20 - 50 ℃; for 10h;
71%
chloroacetone; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 1h; Inert atmosphere;
phosphorous acid trimethyl ester; In acetone; acetonitrile; at 50 ℃; for 24h; Inert atmosphere;
64%
chloroacetone; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 1h;
phosphorous acid trimethyl ester; In acetone; acetonitrile; at 20 - 50 ℃; for 16h;
62%
With potassium iodide; In acetone; acetonitrile; at 20 - 50 ℃; for 10h;
45%
chloroacetone; With potassium iodide; In acetone; acetonitrile; at 20 ℃; for 0.833333h;
phosphorous acid trimethyl ester; With triphenylphosphine; In acetone; acetonitrile; at 20 - 50 ℃; for 17h;
36%
ethyl acetate
141-78-6

ethyl acetate

dimethyl methane phosphonate
756-79-6

dimethyl methane phosphonate

dimethyl (2-oxopropyl)phosphonate
4202-14-6

dimethyl (2-oxopropyl)phosphonate

Conditions
Conditions Yield
dimethyl methane phosphonate; With n-butyllithium; In hexane; toluene; at -80 ℃; for 0.166667h; Inert atmosphere;
ethyl acetate; In hexane; toluene; at -80 ℃; for 1h; Inert atmosphere;
50%
With n-butyllithium; Multistep reaction; 1.) THF, -78 deg C, 15 min, 2.) THF, -78 deg C, 30 min;

2.What is the CAS number for Dimethyl acetylmethylphosphonate ?

The CAS number of Dimethyl acetylmethylphosphonate is 4202-14-6.

More information of Dimethyl acetylmethylphosphonate 4202-14-6 are:

CAS?Number

4202-14-6

Density

1.145 g/cm3

Melting Point

76-79 °C at 3 mm Hg

Boiling Point

227 °C at 760 mmHg

Flash Point

105.3 °C

Vapor Pressure

0.0793mmHg at 25°C

Refractive Index

n20/D 1.439(lit.)

HS CODE

29310095

PSA

62.41000

LogP

1.06130

3.What are another words for Dimethyl acetylmethylphosphonate ?

Synonyms?for?Dimethyl acetylmethylphosphonate 4202-14-6:Phosphonicacid, (2-oxopropyl)-, dimethyl ester (9CI);Phosphonic acid, acetonyl-,dimethyl ester (6CI,7CI,8CI);(2-Oxopropyl)phosphonic acid dimethyl ester;(Dimethylphosphono)acetone;Dimethyl (2-oxopropyl)phosphonate;Dimethylacetonylphosphonate;Dimethyl b-keto-propylphosphonate;

4.What is the molecular formula of Dimethyl acetylmethylphosphonate?

The chemical formula of ?Dimethyl acetylmethylphosphonate is?C5H11O4P which containing 5 Carbon atoms,11 Hydrogen atoms,4 Oxygen atoms and 1 Phosphorus atoms,and the molecular weight of??Dimethyl acetylmethylphosphonate?is 166.114.

5.What is Dimethyl acetylmethylphosphonate (4202-14-6) used for?

Dimethyl acetylmethylphosphonate is an organic compound that serves as a reagent in chemical reactions, particularly in the alkynylation of aldehydes. It is known for its ability to react with tosyl azide in a one-pot process, making it a valuable component in the synthesis of various organic compounds.

InChI:InChI=1/C5H11O4P/c1-5(6)4-10(7,8-2)9-3/h4H2,1-3H3

Relevant articles related to Dimethyl acetylmethylphosphonate:

Article

Source

A Convenient Procedure for the Synthesis of 2,2,2-Trifluoroethyl Methyl 2-Oxoalkylphosphonates

Molnár, Katalin,Behra, Julien,Takács, László,Kádár, Mihály,Kardos, Zsuzsanna,Faigl, Ferenc

, p. 677 - 680 (2015)

Structure-Elucidating Total Synthesis of the (Polyenoyl)tetramic Acid Militarinone C §

Brückner, Reinhard,Drescher, Christian,Hamburger, Matthias,Keller, Morris,Potterat, Olivier

supporting information, (2020/03/30)

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