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O,O,O,O-tetraethylbenzylidenediphosphonate is a chemical compound with the molecular formula C16H25O6P2. It is a white crystalline solid that is soluble in organic solvents. O,O,O,O-tetraethylbenzylidenediphosphonate is characterized by its benzylidene group, which is a carbon-carbon double bond between two carbon atoms, and two phosphonate groups attached to the benzylidene. The tetraethylbenzylidenediphosphonate is used in various applications, including as a flame retardant, a plasticizer, and a stabilizer in the chemical industry. It is also known for its potential use in the synthesis of other organophosphorus compounds. Due to its phosphorus content, it can be effective in enhancing the thermal stability and flame resistance of materials. However, it is important to handle O,O,O,O-tetraethylbenzylidenediphosphonate with care due to its potential environmental and health impacts, and it is subject to regulatory controls regarding its use and disposal.

2530-54-3

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2530-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2530-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2530-54:
(6*2)+(5*5)+(4*3)+(3*0)+(2*5)+(1*4)=63
63 % 10 = 3
So 2530-54-3 is a valid CAS Registry Number.

2530-54-3Downstream Products

2530-54-3Relevant academic research and scientific papers

Studies on organophosphorus compounds 68. A new and facile synthetic approach to alkylidenebisphosphonates

Li, Chaozhong,Yuan, Chengye

, p. 1515 - 1516 (1993)

Condensation of aldehydes with diethyl phosphite followed by sulfonylation of the α-hydroxy group formed with methanesulfonyl chloride and subsequent substitution by another molecule of diethylphosphite provides corresponding alkylidenebisphosphonates in one-pot procedure with good yield.

Synthesis of new functionalized aryl-substituted methylphosphonic and methylenediphosphonic acids and their derivatives

Prishchenko, Andrey A.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Petrosyan, Valery S.

, p. 381 - 388 (2016/12/14)

The convenient syntheses of new aryl-substituted hydroxymethylphosphonic and methylenediphosphonic acids from the aromatic aldehydes, their derivatives, and phosphorous acid esters in the presence of the effective catalysts (trimethylsilyl trifluoromethanesulfonate, zinc chloride, and cadmium iodide) were developed.

Modified Colorants and Inkjet Ink Compositions Comprising Modified Colorants

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Paragraph 0241-0244, (2016/04/09)

The present invention relates to a modified colorant comprising a colorant having attached at least one organic group. Various embodiments of the organic group are disclosed. For each of these embodiments, preferably the organic group has a defined calciu

Bis-phosphonate compounds

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, (2008/06/13)

The present invention provides a pharmaceutical compound, or pharmaceutically acceptable salt thereof, for use in medicine, wherein said compound is of formula I wherein R is a pharmaceutically active moiety; Ar is an aromatic moiety; X is a linker group; and Y is a moiety comprising two phosphonate groups. Further aspects of the invention relate to a method for palliative and curative treatment of bone disorders and cancer related disorders, such as breast cancer.

Bis-phosphonate compounds

-

, (2008/06/13)

The present invention provides a pharmaceutical compound, or pharmaceutically acceptable salt thereof, for use in medicine, wherein said compound is of formula I wherein R is a pharmaceutically active moiety; Ar is an aromatic moiety; X is a linker group; and Y is a moiety comprising two phosphonate groups. Further aspects of the invention relate to a method for palliative and curative treatment of bone disorders and cancer related disorders, such as breast cancer.

ALKYLIDENEDIPHOSPHONATES ET VINYLPHOSPHONATES: UNE DEMARCHE SYNTHETIQUE SELECTIVE PAR VOIE CARBANIONIQUE

Teulade, Marie-Paule,Savignac, Philippe,Aboujaoude, Elie Elia,Lietge, Stephane,Collignon, Noel

, p. 283 - 300 (2007/10/02)

Phosphonoalkylation of acylchloro-phosphates or -phosphinates in the presence of excess lithium diisopropylamide leads to direct generation of lithiated methylenediphosphonate anions.This stable type of anion can be either protonated in acidic medium to provide tetrasubstituted methylenediphosphonate or alkylated.When aliphatic or aromatic aldehydes are added spontaneous formation of vinylphosphonates is observed.This process is a simple and convenient route to diphosphonic as well as to vinylphosphonic compounds.

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