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Fluorooxaloacetic acid diethyl ester, also known as FOE, is a chemical compound with the molecular formula C6H9FNO4. It is a derivative of oxaloacetic acid, where one of the hydrogen atoms is replaced by a fluorine atom, and the carboxylic acid groups are esterified with ethanol. FOE is a colorless liquid with a pungent odor and is soluble in organic solvents. It is primarily used as a herbicide, specifically for the control of broadleaf weeds and grasses in various crops. The compound works by inhibiting the enzyme enolpyruvate carboxylase, which is essential for plant growth, ultimately leading to the death of the targeted weeds. Due to its potential environmental and health risks, the use of FOE is subject to strict regulations in many countries.

392-58-5

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392-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392-58-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 392-58:
(5*3)+(4*9)+(3*2)+(2*5)+(1*8)=75
75 % 10 = 5
So 392-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H11FO5/c1-3-13-7(11)5(9)6(10)8(12)14-4-2/h5H,3-4H2,1-2H3

392-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl 2-fluoro-3-oxosuccinate

1.2 Other means of identification

Product number -
Other names diethyl 2-fluoro-3-oxobutanedioate

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:392-58-5 SDS

392-58-5Relevant academic research and scientific papers

Improved synthesis of d,l-fluorocitric acid

Vardanyan, Ruben,Kumirov, Vlad K.,Hruby, Victor J.

experimental part, p. 920 - 924 (2011/11/12)

We propose a decagram synthesis of commercially unavailable fluorocitric acid. The synthesis begins with benzyl fluoroacetate, which is converted to dibenzyl 2-fluoro-3-oxosuccinate, followed by condensation with malonic acid or its monobenzyl ester and subsequent hydrogenolysis.

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