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CLODINAFOP, also known as (R)-Clodinafop, is an aromatic ether derived from (R)-lactic acid, with its hydroxy group at position 2 converted to the corresponding p-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenyl ether. It serves as the parent acid of the herbicide clodinafop-propargyl and is widely recognized for its effectiveness in controlling weeds.

114420-56-3

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114420-56-3 Usage

Uses

Used in Agricultural Industry:
CLODINAFOP is used as a herbicide for weed control in wheat. It is particularly effective in managing various types of weeds that can hinder the growth and productivity of wheat crops. By targeting specific weed species, CLODINAFOP helps maintain the health and yield of wheat, contributing to more efficient and sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 114420-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114420-56:
(8*1)+(7*1)+(6*4)+(5*4)+(4*2)+(3*0)+(2*5)+(1*6)=83
83 % 10 = 3
So 114420-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClFNO4/c1-8(14(18)19)20-10-2-4-11(5-3-10)21-13-12(16)6-9(15)7-17-13/h2-8H,1H3,(H,18,19)/t8-/m1/s1

114420-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name clodinafop

1.2 Other means of identification

Product number -
Other names UNII-I5VL6U0SD8

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:114420-56-3 SDS

114420-56-3Relevant academic research and scientific papers

HERBICIDAL COMPOSITIONS

-

, (2022/03/02)

The present invention provides compositions comprising herbicidally active compounds (A) and (B), where (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition according to the invention for controlling harmful plants or for regulating growth.

Synthesis method of clodinafop-propargyl

-

Paragraph 0015; 0017; 0019; 0021, (2021/01/29)

The invention relates to the field of chemical engineering, and discloses a synthesis method of clodinafop-propargyl. The method comprises the following steps of: dissolving DHPPA in an organic solvent, heating to a temperature of 50 DEG C, adding an anti

Design, Synthesis and Biological Activity of 2-(4-Aryloxyphenoxy) Propionamides Containing 1,3,4-Thiadiazole

Hui, Yang Zi

, p. 1 - 4 (2021/06/12)

Four new 2-(4-aryloxyphenoxy) propionamides containing 1,3,4-thiadiazole moiety were synthesized based on the structure of Quizalofop-P. The structures of the synthesized compounds were confirmed by 1H nuclear magnetic resonance, elemental analysis, and optical rotation. The herbicidal bioassay showed that the title compounds had good herbicidal activity against barnyard grass.

Phenoxyphenoxypropionic acid ethyl ester compound as well as preparation method and application thereof

-

Paragraph 0041; 0043; 0047; 0048, (2019/08/30)

The invention discloses an ethyl pyridyloxyphenoxypropionate compound as well as a preparation method and application thereof. The compound is a compound with a structure shown as a formula (1) or pharmaceutically acceptable salt thereof. The compound or

Chiral carbon-containing aryloxy phenoxypropanamide compound as well as preparation method and application thereof

-

Paragraph 0024; 0025, (2018/11/22)

The invention discloses a chiral carbon-containing aryloxy phenoxypropanamide compound as well as a preparation method and application thereof. The preparation method comprises the following steps: carrying out a williamson etherification reaction on R-2-

Aryloxy-phenoxy alkane acid derivative and medicinal application thereof

-

Paragraph 0014-0016, (2018/07/30)

The invention discloses an aryloxy-phenoxy alkane acid derivative and a medicinal application thereof. The aryloxy-phenoxy alkane acid derivative is shown as the chemical formula I in the specification, wherein R1 is any one of hydrogen, alkyl containing

Tetrahydro naphthalene-2-aryloxy phenoxy alkyl ketone compound with anti-tumor activity and pharmaceutical application of compound

-

Paragraph 0014-0016, (2018/09/11)

The invention discloses a tetrahydro naphthalene-2-aryloxy phenoxy alkyl ketone compound and a medical application thereof. The chemical structural formula of the compound is as shown in the formula Iin the specification, wherein R1, R2, R3 and R4 are any

Tetrahydroisoquinoline-2-aryloxyphenoxyalkyl ketone compound and application thereof

-

Paragraph 0025; 0026, (2017/07/07)

The invention discloses a tetrahydroisoquinoline-2-aryloxyphenoxyalkyl ketone compound and application thereof. The chemical structural formula of the compound is shown in formula I or II shown in the description, where each of R, R, R and R i

2-(hexahydric aryloxy phenoxy)alkanoic acid derivative and application thereof

-

Paragraph 0024; 0025; 0026, (2017/07/21)

The invention discloses a 2-(hexahydric aryloxy phenoxy)alkanoic acid derivative and application thereof as a herbicide. The chemical formula of the 2-(hexahydric aryloxy phenoxy)alkanoic acid derivative is shown in the specification, wherein R, R,

Pyridyl-3-yl-aryloxyphenoxynoic acid ester compounds and application thereof

-

Paragraph 0024; 0025; 0026, (2017/07/23)

The invention discloses pyridyl-3-yl-aryloxyphenoxynoic acid ester compounds and herbicidal activities thereof. The chemical structural formula is disclosed as Formula I or II, wherein X is nitrogen or carbon; Y is -N=CH- or oxygen; X1, X2 and X3 are resp

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