1-(5-(((2-Cyanoethyl)thio)methyl)thiazol-2-yl)guanidine
95%
- Product Code: 80540
CAS:
131184-89-9
| Molecular Weight: | 241.34 g./mol | Molecular Formula: | C₈H₁₁N₅S₂ |
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| Melting Point: | Boiling Point: | 459.7±55.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily used in research and development within the field of medicinal chemistry. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its structure, featuring a thiazole ring and guanidine group, makes it valuable in designing compounds that interact with specific proteins or enzymes, potentially leading to the development of new therapeutic agents. Researchers explore its applications in creating drugs for conditions such as microbial infections or metabolic disorders, leveraging its ability to modulate biochemical pathways. Additionally, it may be utilized in the study of chemical reactions involving sulfur-containing heterocycles, contributing to advancements in organic synthesis methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,158.00 |
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| 1.000 | 10-20 days | ฿8,325.00 |
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1-(5-(((2-Cyanoethyl)thio)methyl)thiazol-2-yl)guanidine
This compound is primarily used in research and development within the field of medicinal chemistry. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its structure, featuring a thiazole ring and guanidine group, makes it valuable in designing compounds that interact with specific proteins or enzymes, potentially leading to the development of new therapeutic agents. Researchers explore its applications in creating drugs for conditions such as microbial infections or metabolic disorders, leveraging its ability to modulate biochemical pathways. Additionally, it may be utilized in the study of chemical reactions involving sulfur-containing heterocycles, contributing to advancements in organic synthesis methodologies.
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