2-((1-Phenyl-2,5,8,11,14,17,20,23-octaoxapentacosan-25-yl)oxy)tetrahydro-2H-pyran
97%
- Product Code: 106959
CAS:
1611489-00-9
| Molecular Weight: | 544.67 g./mol | Molecular Formula: | C₂₈H₄₈O₁₀ |
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| EC Number: | MDL Number: | MFCD29049395 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Primarily utilized in the field of organic synthesis, this chemical serves as a versatile protecting group for hydroxyl functionalities. Its structure, featuring a polyether chain and a tetrahydropyran moiety, allows for selective protection of alcohols under mild conditions. This is particularly valuable in multi-step synthetic processes where temporary masking of hydroxyl groups is necessary to prevent unwanted reactions. Additionally, its solubility in a range of organic solvents enhances its utility in various reaction environments. The compound is also employed in the development of complex molecules, including pharmaceuticals and natural products, where precise control over functional group reactivity is crucial. Its stability under acidic and basic conditions further broadens its applicability in diverse synthetic strategies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿42,525.00 |
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2-((1-Phenyl-2,5,8,11,14,17,20,23-octaoxapentacosan-25-yl)oxy)tetrahydro-2H-pyran
Primarily utilized in the field of organic synthesis, this chemical serves as a versatile protecting group for hydroxyl functionalities. Its structure, featuring a polyether chain and a tetrahydropyran moiety, allows for selective protection of alcohols under mild conditions. This is particularly valuable in multi-step synthetic processes where temporary masking of hydroxyl groups is necessary to prevent unwanted reactions. Additionally, its solubility in a range of organic solvents enhances its utility in various reaction environments. The compound is also employed in the development of complex molecules, including pharmaceuticals and natural products, where precise control over functional group reactivity is crucial. Its stability under acidic and basic conditions further broadens its applicability in diverse synthetic strategies.
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