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1,5(2H)-Pyrimidinedicarboxylic acid, 6-(3,4-difluorophenyl)-3,6-dihydro-4-(methoxymethyl)-2-oxo-, 5-methyl 1-(4-nitrophenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191353-92-1

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191353-92-1 Usage

Molecular structure

The compound has a complex molecular structure with a pyrimidine ring, two carboxylic acid groups, and various substitutions and functional groups.

Pyrimidine ring

The core structure of the compound is a pyrimidine ring, which is a six-membered heterocyclic ring containing four carbon atoms and two nitrogen atoms.

Carboxylic acid groups

The compound contains two carboxylic acid groups (-COOH) attached to the pyrimidine ring, which can participate in various chemical reactions and interactions.

Esterification

The compound is esterified with a 5-methyl-1-(4-nitrophenyl) group, which is attached to one of the carboxylic acid groups through an ester linkage.

3,6-dihydro-4-(methoxymethyl)-2-oxo-substitution

The compound has a substitution at the 6-position of the pyrimidine ring, which includes a 3,6-dihydro-4-(methoxymethyl)-2-oxo group.

3,4-difluorophenyl substitution

The compound also has a 3,4-difluorophenyl substitution at the 5-position of the pyrimidine ring, which introduces fluorine atoms and affects the compound's properties.

Potential chemical and biological activities

The various functional groups in the compound give it a wide range of potential chemical and biological activities, making it valuable for pharmaceutical and research purposes.

Applications

Due to its complex structure and potential activities, the compound may be used in the development of new drugs, as a research tool, or in the study of biological processes.

Stability

The compound's stability may depend on factors such as temperature, pH, and the presence of other chemicals or enzymes, which can affect its reactivity and potential applications.

Synthesis

The synthesis of this complex compound likely involves multiple steps and the use of various reagents and reaction conditions to introduce the different functional groups and substitutions.

Check Digit Verification of cas no

The CAS Registry Mumber 191353-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,5 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 191353-92:
(8*1)+(7*9)+(6*1)+(5*3)+(4*5)+(3*3)+(2*9)+(1*2)=141
141 % 10 = 1
So 191353-92-1 is a valid CAS Registry Number.

191353-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-3-(4-nitrophenoxycarbonyl)-4-(3,4-difluorophenyl)-6-methoxymethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 5-Methoxycarbonyl-4-methoxymethyl-1,2,3,6-tetrahydro-2-oxo-6(S)-(3,4-difluorophenyl)-1-(4-nitrophenyloxy-carbonyl)pyrimidine

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:191353-92-1 SDS

191353-92-1Relevant academic research and scientific papers

Syntheses of precursors and reference compounds of the melanin- concentrating hormone receptor 1 (MCHR1) Tracers [11C]SNAP-7941 and [18F]FE@SNAP for positron emission tomography

Schirmer, Eva,Shanab, Karem,Datterl, Barbara,Neudorfer, Catharina,Mitterhauser, Markus,Wadsak, Wolfgang,Philippe, Cecile,Spreitzer, Helmut

, p. 12119 - 12143 (2013/11/06)

The MCH receptor has been revealed as a target of great interest in positron emission tomography imaging. The receptor's eponymous substrate melanin-concentrating hormone (MCH) is a cyclic peptide hormone, which is located predominantly in the hypothalamus with a major influence on energy and weight regulation as well as water balance and memory. Therefore, it is thought to play an important role in the pathophysiology of adiposity, which is nowadays a big issue worldwide. Based on the selective and high-affinity MCH receptor 1 antagonist SNAP-7941, a series of novel SNAP derivatives has been developed to provide different precursors and reference compounds for the radiosyntheses of the novel PET radiotracers [11C]SNAP-7941 and [18F] FE@SNAP. Positron emission tomography promotes a better understanding of physiologic parameters on a molecular level, thus giving a deeper insight into MCHR1 related processes as adiposity.

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