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2401-47-0

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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.

2401-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Chlorophenoxy)-N,N-dimethylethanamine

1.2 Other means of identification

Product number -
Other names I01-9578

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:2401-47-0 SDS

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.

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