2401-47-0 Usage
Description
2-(4-chlorophenoxy)-N,N-dimethylethanamine, also known as dimethylaminoethyl 4-chlorophenoxyacetate, is an organic compound belonging to the phenylpropanoid class. It has the chemical formula C10H14ClNO2 and appears as a clear liquid.
Uses
Used in Agricultural Industry:
2-(4-chlorophenoxy)-N,N-dimethylethanamine is used as a herbicide and plant growth regulator for controlling the growth of unwanted plants. It functions by disrupting auxin transport, leading to uncontrolled growth and ultimately causing the death of the targeted plants.
However, its use is regulated in some regions due to potential environmental and health risks, such as the risk of groundwater contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 2401-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2401-47:
(6*2)+(5*4)+(4*0)+(3*1)+(2*4)+(1*7)=50
50 % 10 = 0
So 2401-47-0 is a valid CAS Registry Number.
2401-47-0Relevant articles and documents
Mustard Carbonate Analogues as Sustainable Reagents for the Aminoalkylation of Phenols
Annatelli, Mattia,Trapasso, Giacomo,Salaris, Claudio,Salata, Cristiano,Castellano, Sabrina,Aricò, Fabio
supporting information, p. 3459 - 3464 (2021/05/24)
N,N-dialkyl ethylamine moiety can be found in numerous scaffolds of macromolecules, catalysts, and especially pharmaceuticals. Common synthetic procedures for its incorporation in a substrate relies on the use of a nitrogen mustard gas or on multistep syntheses featuring chlorine hazardous/toxic chemistry. Reported herein is a one-pot synthetic approach for the easy introduction of aminoalkyl chain into different phenolic substrates through dialkyl carbonate (β-aminocarbonate) chemistry. This new direct alcohol substitution avoids the use of chlorine chemistry, and it is efficient on numerous pharmacophore scaffolds with good to quantitative yield. The cytotoxicity via MTT of the β-aminocarbonate, key intermediate of this synthetic approach, was also evaluated and compared with its alcohol precursor.