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24889-11-0

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24889-11-0 Usage

General Description

2-(4-chlorophenoxy)-2-methylpropanenitrile, also known as Fluazifop-P, is a selective herbicide used to control grassy weeds in agricultural and horticultural crops. It belongs to the aryloxyphenoxypropionate class of herbicides and works by inhibiting the enzyme acetyl-CoA carboxylase, which is essential for lipid synthesis in plants. This disruption of lipid production leads to the death of the targeted weeds while leaving the desired crops relatively unaffected. However, it is important to use this chemical with caution as it may have negative impacts on non-target plants and the environment if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 24889-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,8 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24889-11:
(7*2)+(6*4)+(5*8)+(4*8)+(3*9)+(2*1)+(1*1)=140
140 % 10 = 0
So 24889-11-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNO/c1-10(2,7-12)13-9-5-3-8(11)4-6-9/h3-6H,1-2H3

24889-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-CHLOROPHENOXY)-2-METHYLPROPANENITRILE

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:24889-11-0 SDS

24889-11-0Relevant articles and documents

Decarboxylative Cyanation of Aliphatic Carboxylic Acids via Visible-Light Flavin Photocatalysis

Ramirez, Nieves P.,K?nig, Burkhard,Gonzalez-Gomez, Jose C.

supporting information, (2019/03/08)

An operationally simple method is disclosed for the decarboxylative cyanation of aliphatic carboxylic acids at room temperature. Riboflavin tetraacetate, which is an inexpensive organic photocatalyst, promotes the oxidation of carboxylic acids upon visible-light activation. After decarboxylation, the generated radicals are trapped by TsCN, yielding the desired nitriles without any further additive, in a redox-neutral process. Importantly, this protocol can be adapted to flow conditions.

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