Methyl 2-((3-chloropropyl)thio)acetate
95%
- Product Code: 58506
CAS:
62519-33-9
| Molecular Weight: | 182.66 g./mol | Molecular Formula: | C₆H₁₁ClO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20634401 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a thioether and an ester group, makes it a versatile building block in the development of compounds with potential biological activity. It is often employed in the synthesis of sulfur-containing molecules, which are crucial in drug design due to their ability to enhance binding affinity and metabolic stability. Additionally, it can be utilized in the preparation of functionalized polymers or materials, where its reactive groups allow for further modification or cross-linking. Its application extends to research settings, where it serves as a reagent in the study of chemical reactions involving sulfur-containing compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,100.00 |
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| 0.250 | 10-20 days | ฿13,500.00 |
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| 1.000 | 10-20 days | ฿28,800.00 |
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Methyl 2-((3-chloropropyl)thio)acetate
This chemical is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a thioether and an ester group, makes it a versatile building block in the development of compounds with potential biological activity. It is often employed in the synthesis of sulfur-containing molecules, which are crucial in drug design due to their ability to enhance binding affinity and metabolic stability. Additionally, it can be utilized in the preparation of functionalized polymers or materials, where its reactive groups allow for further modification or cross-linking. Its application extends to research settings, where it serves as a reagent in the study of chemical reactions involving sulfur-containing compounds.
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