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 117499-16-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1,7-Bis-Boc-1,4,7-triazaheptane features two tert-butoxycarbonyl groups flanking a linear triazahexane backbone, enabling sequential deprotection and controlled functionalization. This bifunctional scaffold delivers precise access to diamine intermediates under mild conditions, ideal for peptide coupling and macrocyclization strategies in medicinal chemistry workflows.
1,7-Bis-Boc-1,4,7-triazaheptane serves as a versatile bis-protected diamine scaffold for the construction of symmetric and asymmetric triazacyclononane (TACN) derivatives. The Boc groups enable stable storage and orthogonal deprotection, facilitating sequential functionalization. This compound functions as a key building block in ligand design for transition metal catalysis and chelation studies, offering excellent solubility and compatibility with standard peptide coupling protocols.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
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: