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2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]is a versatile organic chemical compound characterized by the molecular formula C11H12N2OS. It integrates both alcohol and pyrimidine functional groups within its structure, which endows it with unique chemical properties. 2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]is widely recognized for its potential in various scientific and industrial applications, particularly in organic synthesis, pharmaceutical research, medicinal chemistry, and even in the emerging fields of materials science and nanotechnology.

157664-66-9

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157664-66-9 Usage

Uses

Used in Pharmaceutical Research:
2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]is utilized as a key intermediate in the synthesis of pharmaceutical compounds, specifically for the development of antiviral and anticancer drugs. Its unique structure allows it to interact with biological targets, making it a promising candidate for the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the realm of organic synthesis, 2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]serves as a valuable building block for the creation of more complex organic molecules. Its functional groups facilitate various chemical reactions, contributing to the synthesis of a wide array of organic compounds.
Used in Medicinal Chemistry:
2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]is employed as a molecular scaffold in medicinal chemistry, where its properties can be fine-tuned to enhance its therapeutic potential. Its ability to be modified and functionalized makes it suitable for the design of new drugs with improved efficacy and selectivity.
Used in Materials Science and Nanotechnology:
2,4-Pentadiyn-1-ol, 5-[4-methyl-2-(methylthio)-5-pyrimidinyl]may also find applications in materials science and nanotechnology due to its unique chemical characteristics. It could be integrated into the development of new materials with specific properties, such as those with enhanced electronic, optical, or catalytic functions.

Check Digit Verification of cas no

The CAS Registry Mumber 157664-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,6,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 157664-66:
(8*1)+(7*5)+(6*7)+(5*6)+(4*6)+(3*4)+(2*6)+(1*6)=169
169 % 10 = 9
So 157664-66-9 is a valid CAS Registry Number.

157664-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methyl-2-methylsulfanylpyrimidin-5-yl)penta-2,4-diyn-1-ol

1.2 Other means of identification

Product number -
Other names 5-(2-methylthio-4-methyl-5-pyrimidinyl)-2,4-pentadiyn-1-ol

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:157664-66-9 SDS

157664-66-9Downstream Products

157664-66-9Relevant academic research and scientific papers

Synthesis and solid-state polymerization of 5-(2-methylthio4-methylpyrimidin-5-yl)penta-2,4-diyn-l-ol and of several of its derivatives

Wang, Jiang-Hong,Shen, Yu-Quan,Yu, Cong-Xuan,Si, Jing-Hai

, p. 1455 - 1460 (2000)

5-(2-Methylthio-4-methylpyrimidin-5-yl)penta-2,4-diyn-1-ol was synthesized by asymmetric coupling, and the corresponding diacetylene monomers were also prepared in good yields. These monomers could be dissolved in common organic solvents. The monomers can be polymerized in the solid state using heat, light or y-radiation. In addition, micro- and macroscopic third-order susceptibilities were measured by the degenerate four-wave mixing (DFWM) method for the yielded polymers. The Royal Society of Chemistry 2000.

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