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Catalog Number:
25572
CAS Number:
60414-59-7
4-Phénylpyrimidine-2-thiol
Purity:
≥ 98 % (HPLC)
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Product Information

4-Phenylpyrimidine-2-thiol is a versatile compound known for its unique thiol functional group, which enhances its reactivity and potential applications in various fields. This compound is recognized for its role in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to act as a ligand in coordination chemistry makes it valuable in catalysis and material science. Researchers have utilized 4-Phenylpyrimidine-2-thiol in the synthesis of novel compounds, showcasing its potential in drug discovery and development. Additionally, its antioxidant properties open avenues for applications in cosmetics and personal care products, where it can contribute to skin health and protection.

The compound's stability and compatibility with various reaction conditions make it an attractive choice for chemists looking to explore new synthetic pathways. Its unique structure allows for the modification and derivatization, leading to a wide range of potential derivatives with tailored properties. Whether in academic research or industrial applications, 4-Phenylpyrimidine-2-thiol stands out as a valuable building block for innovative solutions.

CAS Number
60414-59-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H8N2S
Molecular Weight
188.25
MDL Number
MFCD00239517
PubChem ID
2305657
Melting Point
209-217 ?C
Appearance
Poudre jaune
Conditions
Conserver à 0-8°C
General Information
CAS Number
60414-59-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H8N2S
Molecular Weight
188.25
MDL Number
MFCD00239517
PubChem ID
2305657
Melting Point
209-217 ?C
Appearance
Poudre jaune
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Phenylpyrimidine-2-thiol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific diseases due to its unique thiol group, enhancing bioactivity.
  • Antioxidant Applications: Its antioxidant properties make it valuable in formulations aimed at reducing oxidative stress in biological systems, which is crucial in fields like cosmetics and health supplements.
  • Coordination Chemistry: This chemical is used to create coordination complexes with metals, which are important in catalysis and materials science, providing enhanced stability and reactivity compared to similar compounds.
  • Analytical Chemistry: It acts as a reagent in various analytical methods, helping to detect and quantify metal ions in environmental samples, thus supporting environmental monitoring and safety assessments.
  • Biochemical Research: The compound is employed in studies investigating enzyme inhibition and protein interactions, contributing to the understanding of biochemical pathways and potential therapeutic targets.

Citations