(S)-2-(Tetrahydrofuran-3-yl)acetic acid
97%
- Product Code: 38172
CAS:
146255-26-7
| Molecular Weight: | 130.1418 g./mol | Molecular Formula: | C₆H₁₀O₃ |
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| EC Number: | MDL Number: | MFCD19229760 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
(S)-2-(Tetrahydrofuran-3-yl)acetic acid is primarily utilized in the synthesis of chiral compounds and pharmaceutical intermediates. Its structural features make it a valuable building block in organic chemistry, particularly in the development of drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce chirality into target molecules, which is crucial for creating enantiomerically pure substances with specific biological activities. Additionally, it serves as a precursor in the production of fine chemicals and agrochemicals, where its tetrahydrofuran ring and carboxylic acid group provide versatile reactivity for further functionalization. Its application extends to research and development in medicinal chemistry, where it aids in the design of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,371.00 |
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(S)-2-(Tetrahydrofuran-3-yl)acetic acid
(S)-2-(Tetrahydrofuran-3-yl)acetic acid is primarily utilized in the synthesis of chiral compounds and pharmaceutical intermediates. Its structural features make it a valuable building block in organic chemistry, particularly in the development of drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce chirality into target molecules, which is crucial for creating enantiomerically pure substances with specific biological activities. Additionally, it serves as a precursor in the production of fine chemicals and agrochemicals, where its tetrahydrofuran ring and carboxylic acid group provide versatile reactivity for further functionalization. Its application extends to research and development in medicinal chemistry, where it aids in the design of novel therapeutic agents.
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