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155380-13-5

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155380-13-5 Usage

Uses

Methyl (2E)-[2-(chloromethyl)phenyl)](methoxyimino)acetate is an impurity from the pesticide active ingredient, Trifloxystrobin, a broad-spectrum foliar fungicide used in plant pritection.

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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