2-((tert-Butoxycarbonyl)amino)ethyl 4-methylbenzenesulfonate
97%
- Product Code: 41179
CAS:
158690-56-3
| Molecular Weight: | 315.3852 g./mol | Molecular Formula: | C₁₄H₂₁NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07776965 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a protecting group reagent. It is often employed to protect amine functionalities during complex chemical reactions, particularly in peptide synthesis. The tert-butoxycarbonyl (Boc) group safeguards the amine, preventing unwanted side reactions, and can be selectively removed under mild acidic conditions. Additionally, the tosylate group (4-methylbenzenesulfonate) serves as a good leaving group, facilitating further functionalization or substitution reactions. Its application is crucial in the development of pharmaceuticals and bioactive molecules, where precise control over reaction pathways is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $58.33 |
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2-((tert-Butoxycarbonyl)amino)ethyl 4-methylbenzenesulfonate
This chemical is primarily utilized in organic synthesis as a protecting group reagent. It is often employed to protect amine functionalities during complex chemical reactions, particularly in peptide synthesis. The tert-butoxycarbonyl (Boc) group safeguards the amine, preventing unwanted side reactions, and can be selectively removed under mild acidic conditions. Additionally, the tosylate group (4-methylbenzenesulfonate) serves as a good leaving group, facilitating further functionalization or substitution reactions. Its application is crucial in the development of pharmaceuticals and bioactive molecules, where precise control over reaction pathways is essential.
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