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Diphenyl (1-methylethyl)phosphonate, also known as diphenyl isopropylphosphonate, is an organophosphorus compound with the chemical formula C15H17O2P. It is a colorless, viscous liquid that is soluble in organic solvents. diphenyl (1-methylethyl)phosphonate is primarily used as a flame retardant, plasticizer, and stabilizing agent in various industrial applications, including the production of plastics, rubber, and coatings. It is also employed as a precursor in the synthesis of other organophosphorus compounds. Due to its potential health and environmental risks, handling and disposal of diphenyl (1-methylethyl)phosphonate must be done with proper safety measures and in accordance with local regulations.

1538-72-3

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1538-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1538-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1538-72:
(6*1)+(5*5)+(4*3)+(3*8)+(2*7)+(1*2)=83
83 % 10 = 3
So 1538-72-3 is a valid CAS Registry Number.

1538-72-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [phenoxy(propan-2-yl)phosphoryl]oxybenzene

1.2 Other means of identification

Product number -
Other names O,O-bisphenyl isopropyl phosphonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1538-72-3 SDS

1538-72-3Downstream Products

1538-72-3Relevant academic research and scientific papers

P-Toluenesulfonic acid-Celite as a reagent for synthesis of esters of alkylphosphonic acids under solvent-free conditions

Gupta, Arvind K.,Kumar, Rajesh,Dubey, Devendra K.,Kaushik

, p. 328 - 331 (2008/02/10)

The coupling reaction of alkylphosphonic acids and alcohols on the surface of p-toluenesulfonic acid-Celite under mild and solvent-free conditions gave the corresponding phosphonates in excellent yields. This method provides a useful rapid synthesis of phosphonates for use in the unambiguous identification of chemical warfare agents.

An efficient method for the esterification of phosphonic and phosphoric acids using silica chloride

Sathe, Manisha,Gupta, Arvind K.,Kaushik

, p. 3107 - 3109 (2007/10/03)

Silica chloride is used as an effective heterogeneous catalyst for the rapid esterification of alkyl/aryl phosphonic/phosphoric acids to their corresponding alkyl/aryl phosphonates/phosphates under mild conditions with quantitative yields.

Mild and efficient Cs2CO3-promoted synthesis of phosphonates

Cohen, Richard J.,Fox, Daniel L.,Eubank, Jarrod F.,Salvatore, Ralph Nicholas

, p. 8617 - 8621 (2007/10/03)

A mild and convenient synthesis for phosphonates using cesium carbonate (Cs2CO3), tetrabutylammonium iodide (TBAI) and DMF was developed at room temperature. Numerous dialkyl phosphites were screened using a diverse array of alkyl halides and these reaction conditions were found to be highly efficient producing various phosphonates exclusively in moderate to high yields.

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