(2R,3S)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate
90%
- Product Code: 39940
CAS:
3601-89-6
| Molecular Weight: | 388.84 g./mol | Molecular Formula: | C₂₁H₂₁ClO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00079148 | |
| Melting Point: | Boiling Point: | 518.4°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the pharmaceutical and research sectors as an intermediate in the synthesis of complex organic compounds. Its structure, featuring tetrahydrofuran and benzoate groups, makes it valuable for developing active pharmaceutical ingredients (APIs) and other biologically active molecules. It is often employed in medicinal chemistry for the design and production of drugs targeting specific biological pathways. Additionally, its chloro and methyl groups contribute to its reactivity, enabling its use in controlled chemical reactions to create more specialized derivatives. Researchers also leverage its properties in studies related to drug delivery systems and pharmacokinetics.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off white Crystal to Powder |
| PURITY | 89.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $58.76 |
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| 1.000 | 10-20 days | $124.56 |
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| 5.000 | 10-20 days | $335.51 |
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| 10.000 | 10-20 days | $601.71 |
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(2R,3S)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate
This chemical is primarily utilized in the pharmaceutical and research sectors as an intermediate in the synthesis of complex organic compounds. Its structure, featuring tetrahydrofuran and benzoate groups, makes it valuable for developing active pharmaceutical ingredients (APIs) and other biologically active molecules. It is often employed in medicinal chemistry for the design and production of drugs targeting specific biological pathways. Additionally, its chloro and methyl groups contribute to its reactivity, enabling its use in controlled chemical reactions to create more specialized derivatives. Researchers also leverage its properties in studies related to drug delivery systems and pharmacokinetics.
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