67942-22-7 Usage
Description
N,N''-DIPHENETHYL-MALONAMIDE, with the molecular formula C18H20N2O2, is a chemical compound that serves as an industrial chelating and complexing agent. It is recognized for its capability to sequester metal ions, forming stable complexes that are instrumental in various applications across different industries. Due to its potential toxicity and environmental impact, careful handling is advised.
Uses
Used in Metal Extraction Processes:
N,N''-DIPHENETHYL-MALONAMIDE is used as a chelating agent for the purpose of metal extraction. Its ability to form stable complexes with metal ions makes it a valuable component in this industry, facilitating the efficient separation and recovery of metals.
Used in Insecticides and Pesticides:
In the agricultural sector, N,N''-DIPHENETHYL-MALONAMIDE is utilized as an active ingredient in certain insecticides and pesticides. Its role is to control and manage pests, thereby protecting crops and enhancing agricultural productivity.
Used in Industrial Applications:
Beyond metal extraction and agriculture, N,N''-DIPHENETHYL-MALONAMIDE is also employed in other industrial applications where its complexing properties are beneficial. This includes uses in chemical synthesis and various manufacturing processes that require the stabilization or separation of metal ions.
Check Digit Verification of cas no
The CAS Registry Mumber 67942-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67942-22:
(7*6)+(6*7)+(5*9)+(4*4)+(3*2)+(2*2)+(1*2)=157
157 % 10 = 7
So 67942-22-7 is a valid CAS Registry Number.
67942-22-7Relevant articles and documents
Redox induced oxidative C-C coupling of non-innocent bis(heterocyclo)methanides
Baliyan, Rupal,Dhara, Suman,Huang, Kuo-Wei,Lahiri, Goutam Kumar,Panda, Sanjib
, p. 16647 - 16659 (2021/12/07)
Redox driven C-C bond formation has gained recent attention over the traditional sequence of oxidative addition, insertion and reductive elimination reactions. In this regard, the transient radical mediated diverse reactivity profile of bis(heterocyclo)me
