2-((2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)disulfanyl)ethyl 4-methylbenzenesulfonate
95%
- Product Code: 191742
CAS:
1807512-37-3
| Molecular Weight: | 392.55 g./mol | Molecular Formula: | C₁₆H₂₄O₅S₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28950768 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Used as a key intermediate in organic synthesis, particularly in the preparation of complex disulfide-containing molecules. Its primary application lies in peptide chemistry, where it serves as a protected disulfide bridge precursor, enabling controlled formation of disulfide bonds in peptides and proteins. The tetrahydropyranyl (THP) group acts as a protecting group for alcohols, allowing selective deprotection under mild acidic conditions, while the tosylate moiety provides a good leaving group for nucleophilic substitution reactions. This dual functionality makes it valuable in stepwise synthesis of biologically active molecules, including pharmaceuticals and biochemical probes. It is also employed in the development of conjugated systems for drug delivery and bioconjugation technologies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿45,520.00 |
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2-((2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)disulfanyl)ethyl 4-methylbenzenesulfonate
Used as a key intermediate in organic synthesis, particularly in the preparation of complex disulfide-containing molecules. Its primary application lies in peptide chemistry, where it serves as a protected disulfide bridge precursor, enabling controlled formation of disulfide bonds in peptides and proteins. The tetrahydropyranyl (THP) group acts as a protecting group for alcohols, allowing selective deprotection under mild acidic conditions, while the tosylate moiety provides a good leaving group for nucleophilic substitution reactions. This dual functionality makes it valuable in stepwise synthesis of biologically active molecules, including pharmaceuticals and biochemical probes. It is also employed in the development of conjugated systems for drug delivery and bioconjugation technologies.
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