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15516-38-8

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15516-38-8 Usage

General Description

Phosphonic acid, bis(2-methylphenyl) ester is a chemical compound commonly used as an intermediate in the production of agrochemicals and pharmaceuticals. It is a derivative of phosphorous acid and consists of two methylphenyl groups attached to the phosphorus atom. Phosphonic acid, bis(2-methylphenyl) ester is often employed as a stabilizer and flame retardant in polymers and plastics due to its high thermal stability and excellent resistance to heat and flame. It is also used as a cross-linking agent for natural and synthetic rubber, as well as a chelating agent in metal cleaning and treatment processes. However, it is important to handle this compound with caution as it can be harmful if ingested, inhaled, or absorbed through the skin, and can cause irritation to the eyes and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 15516-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15516-38:
(7*1)+(6*5)+(5*5)+(4*1)+(3*6)+(2*3)+(1*8)=98
98 % 10 = 8
So 15516-38-8 is a valid CAS Registry Number.

15516-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-methylphenoxy)-oxophosphanium

1.2 Other means of identification

Product number -
Other names Phosphonsaeure-di-o-tolylester

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:15516-38-8 SDS

15516-38-8Relevant articles and documents

Synthetic Studies toward (?)-Cleistenolide: Highly Stereoselective Synthesis of New γ-Lactone Subunits

Sartori, Suélen K.,Miranda, Izabel L.,de Matos, Davi A.,Kohlhoff, Markus,Diaz, Marisa A.N.,Diaz-Mu?oz, Gaspar

, p. 757 - 766 (2021/03/17)

This study describes the stereoselective synthesis of two new γ-lactones in 6 and 3 steps and 19 and 32% yield, respectively, directed toward the total synthesis of the natural product (?)-cleistenolide. The starting material was an enantiomerically pure

Z-selective Horner-Wadsworth-Emmons reaction of ethyl (diarylphosphono)acetates using sodium iodide and DBU

Ando, Kaori,Oishi, Tohru,Hirama, Masahiro,Ohno, Hiroaki,Ibuka, Toshiro

, p. 4745 - 4749 (2007/10/03)

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