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4-Hydroxy-2-mercapto-6-methylpyrimidine is a chemical compound with the molecular formula C5H6N2OS. It is a derivative of pyrimidine and a substituted thiophenol, known for its potential applications in various fields.
Used in Pharmaceutical Industry:
4-Hydroxy-2-mercapto-6-methylpyrimidine is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs.
Used in Agrochemical Industry:
4-Hydroxy-2-mercapto-6-methylpyrimidine serves as an intermediate in the synthesis of agrochemicals, playing a role in the production of substances that help protect crops and enhance agricultural productivity.
Used as a Starting Material for Nucleoside Analogs:
4-Hydroxy-2-mercapto-6-methylpyrimidine is used as a starting material for the synthesis of nucleoside analogs, which possess potential antiviral and anticancer properties, indicating its importance in medicinal chemistry.
Used for Antioxidant and Neuroprotective Properties:
Due to its antioxidant and neuroprotective properties, 4-Hydroxy-2-mercapto-6-methylpyrimidine is a potential candidate for therapeutic applications in medicine, particularly for conditions that involve oxidative stress and neurodegeneration.

195-64-2

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195-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195-64-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 195-64:
(5*1)+(4*9)+(3*5)+(2*6)+(1*4)=72
72 % 10 = 2
So 195-64-2 is a valid CAS Registry Number.

195-64-2Downstream Products

195-64-2Relevant academic research and scientific papers

A Novel Strategy for the Synthesis of Oxygenated Phenanthrenes Involving a Combination of Ullmann and McMurry Reactions

Gies, Anne-Elisabeth,Pfeffer, Michel

, p. 3650 - 3654 (1999)

A general synthetic procedure for the preparation of polyoxygenated phenanthrenes from substituted derivatives of benzaldehyde is described. The key compound is a 6,6′-biphenyl-1,1′-dicarboxaldehyde intermediate formed through an ambient temperature Ullmann coupling. The subsequent McMurry condensation gave rise to the phenanthrene in 45-57% yields.

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