What is the Tetraisopropyl methylenediphosphonate?

Tetraisopropyl methylenediphosphonate is Clear colorless to slightly yellow liquid, while it's Molecular Formula is C13H30O6P2. Clear colorless to slightly yellow liquid Tetraisopropyl methylenediphosphonate [T(iPr)MDP] forms a synergistic mixture with hydrogen dicarbollylcobaltate in nitrobenzene which was used in the extraction of europium and americium.It may be used in the synthesis of the following:tetraisopropyl ethenylidenebisphosphonate.tetraisopropyl 4-acetylthiobutane-1,1-diphosphonatetetraisopropyl 2-(3,5-bis(bromomethyl)phenyl)ethane-1,1-diphosphonate

What is the CAS number for Tetraisopropyl methylenediphosphonate?

The CAS number of Tetraisopropyl methylenediphosphonate is 1660-95-3.

What is Tetraisopropyl methylenediphosphonate (1660-95-3) used for?

Tetraisopropyl methylenediphosphonate (IPCP) is a tetraisopropyl ester of methylenediphosphonic acid, serving as an electroneutral ligand. It is synthesized from triisopropyl phosphate and is characterized by its clear colorless to slightly yellow liquid appearance. Powder electron paramagnetic resonance (EPR) studies of tris complexes of Cu(II) complexes with IPCP have been analyzed, showcasing its potential in various applications.InChI:InChI=1/C13H30O6P2/c1-10(2)16-20(14,17-11(3)4)9-21(15,18-12(5)6)19-13(7)8/h10-13H,9H2,1-8H3

What is the Tetraisopropyl methylenediphosphonate?

Tetraisopropyl methylenediphosphonate is Clear colorless to slightly yellow liquid, while it's Molecular Formula is C13H30O6P2. Clear colorless to slightly yellow liquid Tetraisopropyl methylenediphosphonate [T(iPr)MDP] forms a synergistic mixture with hydrogen dicarbollylcobaltate in nitrobenzene which was used in the extraction of europium and americium.It may be used in the synthesis of the following:tetraisopropyl ethenylidenebisphosphonate.tetraisopropyl 4-acetylthiobutane-1,1-diphosphonatetetraisopropyl 2-(3,5-bis(bromomethyl)phenyl)ethane-1,1-diphosphonate

What is the CAS number for Tetraisopropyl methylenediphosphonate?

The CAS number of Tetraisopropyl methylenediphosphonate is 1660-95-3.

What is Tetraisopropyl methylenediphosphonate (1660-95-3) used for?

Tetraisopropyl methylenediphosphonate (IPCP) is a tetraisopropyl ester of methylenediphosphonic acid, serving as an electroneutral ligand. It is synthesized from triisopropyl phosphate and is characterized by its clear colorless to slightly yellow liquid appearance. Powder electron paramagnetic resonance (EPR) studies of tris complexes of Cu(II) complexes with IPCP have been analyzed, showcasing its potential in various applications.InChI:InChI=1/C13H30O6P2/c1-10(2)16-20(14,17-11(3)4)9-21(15,18-12(5)6)19-13(7)8/h10-13H,9H2,1-8H3

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1660-95-3

Product Name：Tetraisopropyl methylenediphosphonate
Molecular Formula：C₁₃H₃₀O₆P₂
Purity：99%
Molecular Weight：344.325

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Product Details

Appearance:Clear colorless to slightly yellow liquid

Top quality factory supply 1660-95-3 Tetraisopropyl methylenediphosphonate at low price

Molecular Formula:C13H30O6P2
Molecular Weight:344.325
Appearance/Colour:Clear colorless to slightly yellow liquid
Vapor Pressure:3.04E-06mmHg at 25°C
Refractive Index:n20/D 1.431(lit.)
Boiling Point:400 °C at 760 mmHg
Flash Point:209.2 °C
PSA：90.68000
Density:1.081 g/cm³
LogP:5.03010

Tetraisopropyl methylenediphosphonate(Cas 1660-95-3) Usage

General Description

Tetraisopropyl methylenediphosphonate (IPCP) is a tetraisopropyl ester of methylenediphosphonic acid. It is an electroneutral ligand, reported to be synthesized from triisopropyl phosphate. Powder electron paramagnetic resonance (EPR) studies of tris complexes of Cu(II) complexes with IPCP has been analyzed.

InChI:InChI=1/C13H30O6P2/c1-10(2)16-20(14,17-11(3)4)9-21(15,18-12(5)6)19-13(7)8/h10-13H,9H2,1-8H3

1660-95-3 Relevant articles

METHOD OF THE SYNTHESIS OF DIALKYL HALOALKYLPHOSPHONATES AND DIALKYL HALOALKYLOXYALKYLPHOSPHONATES

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Page/Page column 19-20, (2012/02/13)

The invention deals with the method of t...

Efficient and 'green' microwave-assisted synthesis of haloalkylphosphonates via the Michaelis-Arbuzov reaction

Jansa, Petr,Holy, Antonin,Dracinsky, Martin,Baszczynski, Ondrej,Cesnek, Michal,Janeba, Zlatko

supporting information; experimental part, p. 882 - 888 (2011/06/20)

This paper deals with a novel, efficient...

Synthesis of methylene bisphosphonates from carbon disulfide and phosphites via desulfurization: A mechanistic study

Heuze,Lemarie,Vazeux,Gulea,Masson,Sene,Jaffres,Alberti,MacCiantelli

experimental part, p. 820 - 829 (2009/12/03)

The reaction of carbon disulfide with an...

Preparation of halohydrocarbyl phosphonic acid diesters

-

Page/Page column 5, (2008/06/13)

In a process for the production of haloh...

1660-95-3 Process route

: 116-17-6
triisopropyl phosphite

: 74-95-3
1,1-dibromomethane

: 1660-95-3
Tetraisopropyl methylenediphosphonate

: 1809-20-7
diisopropyl hydrogenphosphonate

: 513-02-0
triisopropyl phosphate

: 1445-75-6
diisopropyl methanephosphonate

: 3759-39-5
diisopropyl isopropylphosphonate

: 98432-80-5
diisopropyl (bromomethyl)phosphonate

Conditions

Conditions	Yield
In ethylbenzene; xylene; at 125 ℃; for 24h; under 760.051 - 2052.96 Torr; Product distribution / selectivity;	50%

: 75-11-6
diiodomethane

: 116-17-6
triisopropyl phosphite

: 1660-95-3
Tetraisopropyl methylenediphosphonate

: 1809-20-7
diisopropyl hydrogenphosphonate

: 513-02-0
triisopropyl phosphate

: 99709-52-1
diisopropyl (iodomethyl)phosphonate

Conditions

Conditions	Yield
at 90 ℃; for 2h; Microwave irradiation; Inert atmosphere; Neat (no solvent);
at 120 ℃; for 1.5h; Product distribution / selectivity; Microwave irradiation; Inert atmosphere;	73.5 %Chromat. 8.9 %Chromat. 7.4 %Chromat. 5.3 %Chromat.