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"2-{[2-(2,4-dichloro-6-methylphenoxy)ethyl]amino}ethanol" is a complex organic compound with the molecular formula C11H16Cl2NO2. It features a central ethanol (ethanolamine) structure, with a 2,4-dichloro-6-methylphenoxy group attached to the ethyl chain. 2-{[2-(2,4-dichloro-6-methylphenoxy)ethyl]amino}ethanol is characterized by the presence of two chlorine atoms at the 2nd and 4th positions of the phenyl ring, and a methyl group at the 6th position. The molecule also contains an amino group attached to the ethyl chain, which is connected to the central ethanolamine structure. This chemical is known for its potential applications in pharmaceuticals and as a chemical intermediate, particularly in the synthesis of certain drugs and agrochemicals. Its specific properties and reactivity are influenced by the presence of the chlorine atoms and the methyl group, which can affect its solubility, stability, and interaction with other molecules.

5732-98-9

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5732-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5732-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5732-98:
(6*5)+(5*7)+(4*3)+(3*2)+(2*9)+(1*8)=109
109 % 10 = 9
So 5732-98-9 is a valid CAS Registry Number.

5732-98-9SDS

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 2-oxaspiro[4.4]nonan-1-one

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

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More Details:5732-98-9 SDS

5732-98-9Downstream Products

5732-98-9Relevant academic research and scientific papers

Reaction of 3-alkenols with thallium trinitrate: An unexpected and useful ring contraction

Ferraz, Helena M. C.,Santos, Andrea P.,Silva Jr., Luiz F.,Vieira, Tiago De O.

, p. 751 - 762 (2000)

The first thallium trinitrate (TTN) mediated ring contraction of cyclic homoallylic alcohols, using a 1:1 mixture of AcOH and H2O as solvent, is described. The reaction of two of these alcohols with excess of TTN in pentane gave α-spirocyclopentyl-γ-butirolactones in reasonable yields.

Cyclopropylidenecyclanes Oxydation par l'acide peroxycarboximidique

Bertrand, Marcel,Meou, Alain,Tubul, Arlette

, p. 3691 - 3694 (2007/10/02)

The title reaction gives a mixture of four compounds .A 2-cyclohexyllideneoxetane is invoked as intermediary to account for the unusual lactone formation.

A New Spiro-annelation Procedure: Intramolecular Decarboxylative Alkylation of β-Keto-esters

Eilerman, Robert G.,Willis, Brian J.

, p. 30 - 32 (2007/10/02)

A new intramolecular decarboxylative alkylation route to spirocyclic ketones, and its application to the synthesis of (+/-)-β-vetivone and (+/-)-β-vetispirene are described.

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