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4-(2-Thienyl)pyrimidine-2-thiol, also known as 2-Mercapto-4-(2-thienyl)pyrimidine, is a heterocyclic organic compound with the molecular formula C8H6N2S2. It features both nitrogen and sulfur atoms in its structure, making it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. The presence of thienyl and pyrimidine moieties endows 4-(2-Thienyl)pyrimidine-2-thiol with unique chemical properties and potential applications in drug development and crop protection.

175202-75-2

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175202-75-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(2-Thienyl)pyrimidine-2-thiol is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anticancer, antibacterial, and antifungal properties. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(2-Thienyl)pyrimidine-2-thiol serves as a valuable building block for the creation of novel crop protection agents. Its incorporation into the molecular structure of these agents can enhance their pesticidal properties, leading to more effective and targeted solutions for agricultural challenges.
Used in Medicinal Chemistry Research:
4-(2-Thienyl)pyrimidine-2-thiol is utilized as a subject of research in medicinal chemistry, where its potential therapeutic properties are explored. 4-(2-Thienyl)pyrimidine-2-thiol's unique structure and reactivity make it an attractive candidate for the development of new drugs with novel mechanisms of action.
Used in Agricultural Chemistry Research:
4-(2-Thienyl)pyrimidine-2-thiol is also a focus of research in agricultural chemistry, where its potential as a building block for new agrochemicals is investigated. The exploration of its properties and reactivity can lead to the discovery of innovative crop protection agents with improved performance and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 175202-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175202-75:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*2)+(2*7)+(1*5)=122
122 % 10 = 2
So 175202-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2S2/c11-8-9-4-3-6(10-8)7-2-1-5-12-7/h1-5H,(H,9,10,11)

175202-75-2SDS

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-thiophen-2-yl-1H-pyrimidine-2-thione

1.2 Other means of identification

Product number -
Other names 4-(2-THIENYL)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:175202-75-2 SDS

175202-75-2Downstream Products

175202-75-2Relevant academic research and scientific papers

Syntheses, crystal structures and photophysical properties of d10 transition-metal (Ag+, Cu+, Cd2+ and Zn2+) coordination complexes based on a thiophene-containing heterocyclic thioamide

Wei, Yu-Zhen,Cheng, Zheng,Li, Wei,Zhu, Hai-Bin

, p. 2900 - 2915 (2017)

Four d10 transition-metal coordination complexes 1–4 (1: [Ag2(TPT)2(TPTH)2]; 2: [Cu6(TPT)6]·2DMF; 3: [Cd(TPT)2(TPTH)]·CH3CH2OH, 4: [Zn(TPT)2]n) have been constructed from a newly designed heterocyclic thioamide ligand, TPTH (TPTH?=?4-(thiophen-2-yl)-pyrimidine-2-thiol). All complexes have been structurally elucidated by single crystal X-ray diffraction analyses. Except for 4, which shows a one-dimensional (1-D) chain structure, 1–3 are all discrete coordination complexes featuring dinuclear, hexanuclear and mononuclear entities, respectively. Their photophysical properties have been evaluated in the solid state at room temperature by UV–vis diffuse reflectance and luminescence spectra. Among them, 2 exhibits a strong red luminescence (λem?=?699?nm) with a remarkable red-shift of the maximum emission compared to that of the TPTH ligand (λem?=?536?nm). The red emission observed with 2 is ascribed to a LMCT (ligand-to-metal charge transfer) transition which agrees with the DFT calculations.

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