(S)-(Tetrahydrofuran-3-yl)methanol
97%
- Product Code: 113844
CAS:
124391-75-9
Molecular Weight: | 102.13 g./mol | Molecular Formula: | C₅H₁₀O₂ |
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EC Number: | MDL Number: | MFCD17015961 | |
Melting Point: | Boiling Point: | 198.6±0.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
(S)-(Tetrahydrofuran-3-yl)methanol is widely used in the synthesis of pharmaceuticals, particularly as a chiral building block in the production of active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are essential for drugs with specific biological activities. This compound is also utilized in the development of agrochemicals, where its structure contributes to the efficacy and selectivity of pesticides or herbicides. Additionally, it serves as an intermediate in organic synthesis, enabling the creation of complex molecules for research and industrial applications. Its versatility in chemical reactions, such as oxidation, reduction, and coupling, makes it a key component in various synthetic pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | €267.12 |
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1.000 | 10-20 days | €796.60 |
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(S)-(Tetrahydrofuran-3-yl)methanol
(S)-(Tetrahydrofuran-3-yl)methanol is widely used in the synthesis of pharmaceuticals, particularly as a chiral building block in the production of active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are essential for drugs with specific biological activities. This compound is also utilized in the development of agrochemicals, where its structure contributes to the efficacy and selectivity of pesticides or herbicides. Additionally, it serves as an intermediate in organic synthesis, enabling the creation of complex molecules for research and industrial applications. Its versatility in chemical reactions, such as oxidation, reduction, and coupling, makes it a key component in various synthetic pathways.
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