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4-(3-ethoxy-2-methyl-3-oxopropyl)morpholin-4-ium is a complex organic compound with the molecular formula C10H19NO4. It is a derivative of morpholine, a heterocyclic organic compound with a five-membered ring containing two oxygen atoms and one nitrogen atom. The compound features a 3-ethoxy-2-methyl-3-oxopropyl group attached to the 4-position of the morpholine ring, which contributes to its unique chemical properties. This specific arrangement of atoms and functional groups endows the compound with potential applications in various chemical and pharmaceutical industries, such as the synthesis of intermediates for drug development or the production of specialty chemicals. However, further research and characterization are required to fully understand its properties and potential uses.

6814-72-8

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6814-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6814-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6814-72:
(6*6)+(5*8)+(4*1)+(3*4)+(2*7)+(1*2)=108
108 % 10 = 8
So 6814-72-8 is a valid CAS Registry Number.

6814-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methyl-3-morpholin-4-ium-4-ylpropanoate

1.2 Other means of identification

Product number -
Other names 8-Aethyl-3exo-benzoyloxy-nortropan

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:6814-72-8 SDS

6814-72-8Downstream Products

6814-72-8Relevant academic research and scientific papers

Synthesis of tropeines and allosteric modulation of ionotropic glycine receptors

Maksay, Gabor,Nemes, Péter,Biró, Tímea

, p. 6384 - 6391 (2007/10/03)

Twenty esters of 3α- and 3β-hydroxy(nor)tropanes and two amides of 3α-aminotropane were prepared with substituted benzoic acids. These (nor)tropeines inhibited [3H]strychnine binding to glycine receptors in synaptosomal membranes of rat spinal cord. A ternary allosteric model was applied to determine the dissociation constants (KA) of the tropeines having strong negative cooperativities with [3H]strychnine binding (α > 10). KA values about 10 nM are well below those of known allosteric agents. Low concentrations (0.1KA) of the (nor)tropeines potentiated the displacing effects of glycine. Positive cooperativity with glycine (β1) decreased with the increase in concentration and binding affinity of tropeines. Displacing potencies were also measured for [3H]granisetron binding to 5-HT3 type serotonin receptors of rat cerebral cortex. Selectivities to glycine receptors versus 5-HT3 receptors varied within 4 orders of magnitude. Nortropeines might serve as a lead to high-affinity selective allosteric modulators of glycine receptors.

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