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Ethanamine, 2-(2-methoxyphenoxy)-N-[2-(2-methoxyphenoxy)ethyl]-, also known as 2-(2-methoxyphenoxy)-N-[2-(2-methoxyphenoxy)ethyl]ethanamine, is a complex organic compound with the molecular formula C16H23NO3. It is a derivative of ethanamine, featuring two 2-methoxyphenoxy groups attached to the nitrogen and ethyl chain, respectively. This chemical is characterized by its amine group, which is a key functional group in many biologically active molecules. It is a colorless to pale yellow liquid with a molecular weight of 273.36 g/mol. The compound is not expected to be highly toxic, but it is essential to handle it with care due to its potential irritant properties. It is used in various chemical and pharmaceutical applications, particularly in the synthesis of certain drugs and agrochemicals.

3258-70-6

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3258-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3258-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,5 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3258-70:
(6*3)+(5*2)+(4*5)+(3*8)+(2*7)+(1*0)=86
86 % 10 = 6
So 3258-70-6 is a valid CAS Registry Number.

3258-70-6SDS

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 bis-[2-(2-methoxy-phenoxy)-ethyl]-amine

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:3258-70-6 SDS

3258-70-6Relevant academic research and scientific papers

Design, Synthesis, and Biological Evaluation of a New Series of Carvedilol Derivatives That Protect Sensory Hair Cells from Aminoglycoside-Induced Damage by Blocking the Mechanoelectrical Transducer Channel

O'Reilly, Molly,Kirkwood, Nerissa K.,Kenyon, Emma J.,Huckvale, Rosemary,Cantillon, Daire M.,Waddell, Simon J.,Ward, Simon E.,Richardson, Guy P.,Kros, Corné J.,Derudas, Marco

, p. 5312 - 5329 (2019/06/07)

Aminoglycosides (AGs) are broad-spectrum antibiotics used for the treatment of serious bacterial infections but have use-limiting side effects including irreversible hearing loss. Here, we assessed the otoprotective profile of carvedilol in mouse cochlear cultures and in vivo zebrafish assays and investigated its mechanism of protection which, we found, may be mediated by a block of the hair cell's mechanoelectrical transducer (MET) channel, the major entry route for the AGs. To understand the full otoprotective potential of carvedilol, a series of 18 analogues were prepared and evaluated for their effect against AG-induced damage as well as their affinity for the MET channel. One derivative was found to confer greater protection than carvedilol itself in cochlear cultures and also to bind more tightly to the MET channel. At higher concentrations, both carvedilol and this derivative were toxic in cochlear cultures but not in zebrafish, suggesting a good therapeutic window under in vivo conditions.

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