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Acetic acid, (2,4-dichlorophenoxy)-, (dimethoxyphosphinyl)phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215655-78-0

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215655-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215655-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,5 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 215655-78:
(8*2)+(7*1)+(6*5)+(5*6)+(4*5)+(3*5)+(2*7)+(1*8)=140
140 % 10 = 0
So 215655-78-0 is a valid CAS Registry Number.

215655-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-Dichloro-phenoxy)-acetic acid (dimethoxy-phosphoryl)-phenyl-methyl ester

1.2 Other means of identification

Product number -
Other names -

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:215655-78-0 SDS

215655-78-0Relevant academic research and scientific papers

Synthesis and herbicidal activities of sodium hydrogen 1-(substituted phenoxyacetoxy)alkylphosphonates

Long, Qingwu,Deng, Xiaoyan,Gao, Yujiao,Xie, Huayong,He, Hongwu,Peng, Hao

, p. 819 - 825 (2013/08/23)

A series of sodium hydrogen 1-(substituted phenoxyacetoxy) alkylphosphonates was designed and synthesized. The test for herbicidal activity indicated that most of the phosphonates (8) possessed excellent postemergence herbicidal activities against broadleaf weeds. Especially, 8f and 8g showed the best herbicidal activity against rape and amaranth with more than 95% inhibitory rate. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

Synthesis and herbicidal activities of lithium or potassium hydrogen 1-(substituted phenoxyacetoxy)alkylphosphonates

Peng, Hao,Long, Qingwu,Deng, Xiaoyan,He, Hongwu

, p. 1868 - 1874 (2013/11/06)

A series of lithium or potassium hydrogen 1-(substituted phenoxyacetoxy)alkylphosphonates were designed and synthesized. All the title compounds were identified by IR, 1H NMR, and 31P NMR, some of them were further analyzed by MS and elemental analyses. The test for herbicidal activity indicated that most of the phosphonates (8) possessed excellent postemergence herbicidal activities against broadleaf weeds. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

Simple and improved preparation of α-oxophosphonate monolithium salts

Wang, Tao,Hong, Wu He

, p. 2081 - 2089 (2007/10/03)

Some α-OxoPhosphonate monolithium salts were synthesized by a facile one-step procedure. In this way, α-(2,4-dichlorophenoxyacetoxy)alkyl phosphonic acid dimethyl esters 5 can be transformed into the corresponding phosophonate monolithium salts 6 without influence on the carboxylic ester group under mild conditions.

An efficient synthesis of α-(2,4-dichlorophenoxyacetoxy)aryl methyl phosphonate monosodium salts

Wang, Tao,He, Hong Wu

, p. 1415 - 1423 (2007/10/03)

A series of α-(2,4-dichlorophenoxyacetoxy)aryl methyl phosphonate monosodium salts 6 were synthesized by the reaction of the intermediate 5 with sodium iodide under moderate condition. This method was applied to the synthesis of novel phosphonate derivati

Synthesis and dealkylation of 1 -(dichloro-phenoxyacetoxy) alkyl phosphonates

He, Hongwu,Liu, Xufeng,Hu, Liming,Wang, Siquan,Liu, Zhaojie

, p. 633 - 636 (2007/10/03)

Using the silylation procedure with chlorotrimethylsilane/sodium iodide followed by alcoholysis, 1-(dichlorophenoxy acetoxy)alkyl phosphonic acid dimethyl esters can be transformed into the parent phosphonic acids without influence on carboxylate ester group.

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