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4(1H)-Pyrimidinone, 2-ethyl(9CI) is a heterocyclic chemical compound belonging to the pyrimidine class of organic compounds. It features a six-membered ring structure with four carbon atoms, two nitrogen atoms, and one oxygen atom, characterized by the molecular formula C6H6N2O and a molecular weight of 126.13 g/mol. This versatile compound is recognized for its applications in the synthesis of pharmaceuticals, agrochemicals, dyes, pigments, and other organic compounds, making it a valuable asset in the field of organic chemistry.

14331-50-1

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14331-50-1 Usage

Uses

Used in Pharmaceutical Industry:
4(1H)-Pyrimidinone, 2-ethyl(9CI) serves as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of drugs targeting a wide range of therapeutic areas, including antiviral, anticancer, and anti-inflammatory treatments. 4(1H)-Pyrimidinone, 2-ethyl(9CI)'s ability to form stable complexes with biological targets makes it an essential component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4(1H)-Pyrimidinone, 2-ethyl(9CI) is utilized in the production of pesticides and herbicides. Its chemical properties enable the creation of effective compounds that protect crops from pests and diseases, thereby ensuring increased agricultural productivity and crop protection.
Used in Dye and Pigment Industry:
4(1H)-Pyrimidinone, 2-ethyl(9CI) is also employed in the synthesis of dyes and pigments for various applications, such as textiles, plastics, and printing inks. Its ability to impart vibrant colors and excellent stability under different conditions makes it a preferred choice for colorants in these industries.
Used in Organic Synthesis:
Beyond its direct applications, 4(1H)-Pyrimidinone, 2-ethyl(9CI) is a valuable building block in organic synthesis. Its reactivity and functional group compatibility make it suitable for the preparation of a wide array of organic compounds, contributing to the advancement of chemical research and the development of new materials.

Check Digit Verification of cas no

The CAS Registry Mumber 14331-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,3 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14331-50:
(7*1)+(6*4)+(5*3)+(4*3)+(3*1)+(2*5)+(1*0)=71
71 % 10 = 1
So 14331-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O/c1-2-5-7-4-3-6(9)8-5/h3-4H,2H2,1H3,(H,7,8,9)

14331-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-1H-pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names 2-Aethyl-pyrimidin-4-on

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:14331-50-1 SDS

14331-50-1Downstream Products

14331-50-1Relevant academic research and scientific papers

PYRIMIDINE DERIVATIVES AS MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS

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Page/Page column 330-331, (2008/06/13)

The present invention relates to compounds of Formula (I) as modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Regulator (“CFTR”), compositions thereof, and methods therewith. The present invention also relates to methods of treating ABC transporter mediated diseases using such modulators.

A Facile Method for the Preparation of 2-Substituted Pyrimidin-4(3H)-ones by a Retro-Diels-Alder Reaction

Stajer, Geza,Szabo, Angela E.,Bernath, Gabor,Sohar, Pal

, p. 290 - 292 (2007/10/02)

diexo-3-Aza-4-oxotricyclo2.5>non-7-ene (1) reacted with carboximidic esters by ring expansion to yield tricyclic 5,6-dihydropyrimidin-4(3H)-ones 3; when the latter were refluxed in chlorobenzene solution, cyclopentadiene split off to gi

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