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6-methyl-2-(morpholin-4-yl)pyrimidin-4(1H)-one is a chemical compound with the molecular formula C10H13N3O2. It is a derivative of pyrimidin-4(1H)-one, featuring a methyl group at the 6th position and a morpholin-4-yl group at the 2nd position. 6-methyl-2-(morpholin-4-yl)pyrimidin-4(1H)-one is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. Its structure allows for the exploration of different pharmacological properties, making it a valuable intermediate in the development of new drugs. The compound's unique combination of functional groups also makes it a subject of interest for researchers studying the structure-activity relationships of pyrimidine-based compounds.

5340-56-7

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5340-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5340-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5340-56:
(6*5)+(5*3)+(4*4)+(3*0)+(2*5)+(1*6)=77
77 % 10 = 7
So 5340-56-7 is a valid CAS Registry Number.

5340-56-7SDS

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 ethyl 2-bromooctadecanoate

1.2 Other means of identification

Product number -
Other names 2-bromo-octadecanoic acid ethyl ester

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:5340-56-7 SDS

5340-56-7Relevant academic research and scientific papers

Synthesis of an Amphiphilic Bis-Aqua Gd(OBETA) Complex for the Preparation of High-Relaxivity Supramolecular Magnetic Resonance Imaging Probes

Negri, Roberto,Carniato, Fabio,Botta, Mauro,Giovenzana, Giovanni B.,Tei, Lorenzo

, p. 235 - 241 (2016)

Prompted by the favourable relaxometric, thermodynamic and kinetic properties of the bis-hydrated Gd(OBETA) (OBETA=2,2′-oxybis(ethylamine)-N,N,N′,N′-tetraacetic acid) complex, a novel derivative tailored with an n-hexadecyl chain was synthesised. The amphiphilic gadolinium complex was designed and prepared with the aim of obtaining high relaxivity supramolecular aggregates by self-assembly in micelles and liposomes. Thus, lipidic nanoparticles were prepared and characterised by dynamic light scattering and 1H NMR relaxometry. Relaxivity values of up to 48.3 mm-1 s-1 (20 MHz and 298 K) were registered in liposomal aggregates. The binding to human serum albumin (HSA), evaluated both in terms of affinity and relaxometric properties of the supramolecular adduct, yielded exceptionally high relaxivity values (71.4 mm-1 s-1 at 30 MHz and 298 K).

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