1,3-Dioxo-1H-benzo[de]isoquinolin-2(3H)-yl trifluoromethanesulfonate
97%
- Product Code: 52429
CAS:
85342-62-7
| Molecular Weight: | 345.25 g./mol | Molecular Formula: | C₁₃H₆F₃NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02683478 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile reagent. It is particularly effective in introducing the trifluoromethanesulfonate (triflate) group into organic molecules, which is a key step in various catalytic processes. The compound is often employed in the preparation of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to facilitate nucleophilic substitution reactions. Additionally, it is used in the synthesis of polymers and advanced materials, where the triflate group can enhance the properties of the final product. Its application extends to the field of medicinal chemistry, where it aids in the development of new drug candidates by enabling the modification of molecular structures to improve efficacy and selectivity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light yellow powder to crystal |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $112.51 |
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| 5.000 | 10-20 days | $450.53 |
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| 10.000 | 10-20 days | $858.86 |
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| 25.000 | 10-20 days | $2,008.04 |
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1,3-Dioxo-1H-benzo[de]isoquinolin-2(3H)-yl trifluoromethanesulfonate
This chemical is primarily utilized in organic synthesis as a versatile reagent. It is particularly effective in introducing the trifluoromethanesulfonate (triflate) group into organic molecules, which is a key step in various catalytic processes. The compound is often employed in the preparation of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to facilitate nucleophilic substitution reactions. Additionally, it is used in the synthesis of polymers and advanced materials, where the triflate group can enhance the properties of the final product. Its application extends to the field of medicinal chemistry, where it aids in the development of new drug candidates by enabling the modification of molecular structures to improve efficacy and selectivity.
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