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N,N-diethyl-2-(pyridin-2-yloxy)ethanamine is an organic compound with the molecular formula C11H18N2O. It is a derivative of ethanamine, featuring a pyridin-2-yloxy group attached to the ethanamine backbone. This chemical is characterized by its two diethylamine groups (N,N-diethyl) and a pyridine-2-yloxy substituent, which contributes to its unique chemical properties. It is a colorless liquid at room temperature and is soluble in organic solvents. The compound has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its ability to form stable complexes with metal ions. Its chemical structure and reactivity make it a valuable intermediate in the preparation of various organic compounds.

6272-34-0

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6272-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6272-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6272-34:
(6*6)+(5*2)+(4*7)+(3*2)+(2*3)+(1*4)=90
90 % 10 = 0
So 6272-34-0 is a valid CAS Registry Number.

6272-34-0SDS

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 N,N-diethyl-2-pyridin-2-yloxyethanamine

1.2 Other means of identification

Product number -
Other names 2-(2'-diethylamino-ethanoxy)pyridine

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:6272-34-0 SDS

6272-34-0Downstream Products

6272-34-0Relevant academic research and scientific papers

Pharmacological evaluation of some new 2-substituted pyridine derivatives

Narendar, Parasuraman,Parthiban, Jeyaraman,Anbalagan, Navaneetharaman,Gunasekaran, Vedachalam,Thomas Leonard, Joseph

, p. 182 - 187 (2003)

In the present study, a series of 2-substituted-pyridines were synthesized and characterized by IR, 1H-NMR and Elemental Analysis. The compounds were assayed against seizures induced by maximal electro shock (MES) and pentylenetetrazole (scMet). Neurologic deficit was evaluated by the rotarod test. The decrease in the elevated motor activity by introceptive chemical stimuli (amphetamine antagonistic activity) was studied at the dose level of 25 and 50 mg/kg, antihistaminic and cardiac activity were also studied. All the compounds exhibited significant anticonvulsant activity. Compounds 2-(2′-piperazino-ethanoxy)pyridine, 2-(3′-morpholino-2′- hydroxypropyloxy)pyridine, 2-(3′-piperidino-2′-hydroxypropyloxy) pyridine and 2-(3′-piperazino-2′-hydroxypropyloxy)pyridine were most active of the series against MES-induced seizures. Compounds 2-(2′-piperazino-ethanoxy)pyridine, 2-(2′-phenylamino-ethanoxy) pyridine, 2-(3′-imidazolo-2′-hydroxypropyloxy)pyridine, 2-(3′-methylamino-2′-hydroxypropyloxy)pyridine and 2-(3′-piperidino-2′-hydroxypropyloxy)pyridine exhibited significant decrease in the elevated motor activity at the dose of 50 mg/kg. Remarkable sympathetic blocking activity was observed with 2-(3′-piperazino-2′- hydroxypropyloxy)pyridine, 2-(3′-piperidino-2′-hydroxypropyloxy) pyridine and 2-(3′-imidazolo-2′-hydroxypropyloxy)pyridine only. Compounds 2-(2′-morpholino-ethanoxy)pyridine, 2-(2′-piperidino- ethanoxy)pyridine, 2-(2′-piperazino-ethanoxy)pyridine, 2-(2′-imidazolo-ethanoxy)pyridine, 2-(2′-diphenylamino-ethanoxy) pyridine, 2-(2′-diethanolamino-ethanoxy)pyridine, 2-(2′-phenylamino- ethanoxy)pyridine and 2-(2′-(4″-hydroxy)phenylamino-ethanoxy) pyridine exhibited significant blocking of histamine induced contraction on guinea pig ileum.

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