Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 1472656-81-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This sulfonate ester features a tert-butoxycarbonyl-protected amine tethered via an octyl linker to a 4-methylbenzenesulfonate group, enabling orthogonal functionalization in peptide synthesis and bioconjugation workflows. The Boc moiety ensures stability during coupling steps, while the sulfonate acts as a robust leaving group under mild conditions.
8-((tert-Butoxycarbonyl)amino)octyl 4-methylbenzenesulfonate serves as a versatile protected amine building block for peptide and peptidomimetic synthesis. The tert-butoxycarbonyl (Boc) group provides stable protection under acidic conditions, while the p-toluenesulfonate leaving group enables efficient displacement reactions. This reagent facilitates straightforward alkylation of nucleophiles and is compatible with standard purification methods, offering reliable functionality in multi-step synthetic sequences.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: