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155380-13-5

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155380-13-5 Usage

Description

Methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate is a chemical compound that is identified as an impurity derived from the synthesis of the pesticide active ingredient, Trifloxystrobin. methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate possesses a unique chemical structure that includes a chloromethyl group attached to a phenyl ring, with an acetate group and a methoxyimino group connected to the same carbon atom. The compound's chemical properties and reactivity are influenced by these functional groups, which may have potential applications in various fields.

Uses

Used in Pesticide Industry:
Methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate is used as an impurity in the production of Trifloxystrobin, a broad-spectrum foliar fungicide. Its presence in the synthesis process is significant as it can impact the overall quality and efficacy of the final product. The compound's role in the pesticide industry is to serve as a marker for the synthesis process, helping to ensure that the active ingredient meets the required standards for plant protection.
In the context of the provided materials, the primary use of methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate is related to its origin as an impurity in the synthesis of the fungicide Trifloxystrobin. While it may not have direct applications in other industries, its presence and management in the pesticide industry are crucial for maintaining the effectiveness and safety of the final product used in plant protection. Further research and development may reveal additional applications or uses for this compound in various fields, but as of now, its primary significance lies in its role in the pesticide industry.

Check Digit Verification of cas no

The CAS Registry Mumber 155380-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,8 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155380-13:
(8*1)+(7*5)+(6*5)+(5*3)+(4*8)+(3*0)+(2*1)+(1*3)=125
125 % 10 = 5
So 155380-13-5 is a valid CAS Registry Number.

155380-13-5SDS

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 2-[2-(chloromethyl)phenyl]-2-ethoxyiminoacetate

1.2 Other means of identification

Product number -
Other names 2-[2-(chloromethyl)phenyl]-2-ethoxyimino-ethanoate

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:155380-13-5 SDS

155380-13-5Relevant articles and documents

Kresoxim-methyl Derivatives: Synthesis and Herbicidal Activities of (Pyridinylphenoxymethylene)phenyl Methoxyiminoacetates

Cao, Yang-Yang,Mao, Da-Jie,Wang, Wei-Wei,Du, Xiao-Hua

, p. 6114 - 6121 (2017/08/16)

A series of new kresoxim-methyl derivatives, (pyridinylphenoxymethylene)phenyl methoxyiminoacetates, were synthesized and their structures were confirmed by NMR and high-resolution mass spectrometry (HRMS). Although derived from a fungicide, the bioassays indicated that several new compounds had good herbicidal activities. At 37.5 g a.i./ha, compound 5c showed 100% inhibition against Abutilon theophrasti, Amaranthus retroflexus, and Eclipta prostrata, which was better than mesotrione. Compound 5e had a broad herbicidal spectrum against broadleaf weeds. The present work indicates that 5c and 5e may serve as new candidates for potential herbicides.

Preparation of halomethylbenzoyl cyanides

-

, (2008/06/13)

Halomethylbenzoyl cyanides I where Ph is phenyl which is substituted by chloromethyl or bromomethyl and may cary 1-4 other rradicals, are prepared from halomethylbenzoyl chlorides II by reacting II with a cyanide-donating compound in the presence

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