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4-Pyridin-4-ylpyrimidine-2(1H)-thione is a heterocyclic chemical compound with the molecular formula C9H6N4S. It features both pyridine and pyrimidine rings, along with a thione functional group. 4-Pyridin-4-ylpyrimidine-2(1H)-thione holds promise in various fields, particularly in medicinal chemistry for the development of pharmaceuticals, due to its intriguing biological activities.

874779-72-3

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874779-72-3 Usage

Uses

Used in Pharmaceutical Development:
4-Pyridin-4-ylpyrimidine-2(1H)-thione is utilized as a key component in drug discovery for its potential to exhibit significant biological activities. Its unique structure allows it to interact with various biological targets, making it a valuable candidate for the creation of new medications.
Used in Agricultural Chemicals:
In the agricultural sector, 4-Pyridin-4-ylpyrimidine-2(1H)-thione may serve as a building block for the development of novel agrochemicals. Its properties could be harnessed to create compounds that address specific needs in crop protection and enhancement.
Used in Materials Science:
4-Pyridin-4-ylpyrimidine-2(1H)-thione also has potential applications in materials science. It can be employed in the synthesis of innovative polymers and other materials, contributing to the advancement of material technologies and potentially leading to new products with improved properties.

Check Digit Verification of cas no

The CAS Registry Mumber 874779-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,7,7 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 874779-72:
(8*8)+(7*7)+(6*4)+(5*7)+(4*7)+(3*9)+(2*7)+(1*2)=243
243 % 10 = 3
So 874779-72-3 is a valid CAS Registry Number.

874779-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-pyridin-4-yl-1H-pyrimidine-2-thione

1.2 Other means of identification

Product number -
Other names 4-(4-PYRIDINYL)PYRIMIDINE-2-THIOL

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:874779-72-3 SDS

874779-72-3Downstream Products

874779-72-3Relevant academic research and scientific papers

A highly selective fluorescent probe based on coumarin and pyrimidine hydrazide for Cu2+ ion detection

Zhu, Lin,Yang, Xiqiang,Luo, Xubiao,Hu, Bin,Huang, Wei

, (2020/02/15)

A novel diethylamino coumarin Schiff base modified with a pyrimidine-hydrazide (EDMP) was synthesized as Cu2+ fluorescent probe. Its photophysical properties and recognition ability to Cu2+ were studied by UV–Vis, fluorescence, IR and mass spectrum. Under UV light, EDMP probe showed a strong bright green fluorescence. After introducing Cu2+, the probe solution was changed from light green to orange and the maximum absorption wavelength bathochromically shifted from 445 nm to 475 nm. Meanwhile, fluorescence quenching phenomenon was observed. Fluorescence titration experiment showed that EDMP exclusively reacted with Cu2+ and the stoichiometric ratio was 1:1. The lowest detection limit was calculated to be 1.153 μM by fitting the titration curve. Additionally, DFT calculation method was utilized to analyze the action mechanism of EDMP toward Cu2+.

Synthesis and antibacterial activity of a series of heterocyclic sulfonate ligands and their metal complexes

Dong, Hua-Ze,Feng, Xiao-Jun,Dai, Bi-Sheng,Su, Cheng-Bai,Zheng-Zheng,Wang, Lin

, p. 2035 - 2037 (2013/05/09)

A series of heterocyclic sulfonate ligands and their barium(II), silver(I), manganese(II), zinc(II) and cobalt(II) coordination compounds have been synthesized. Through antibacterial activities experiments of these complex compounds, metal salts as well as ligands, the rational conclusion is arrived that antibacterial activities of these compounds come from metal ions.

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