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 1158759-45-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This azetidine derivative features a tert-butoxycarbonyl-protected amine and a cyano group at the 3-position, enabling direct incorporation into peptide synthesis. The strained azetidine ring enhances reactivity in coupling reactions, while the carbamate moiety provides stability under standard conditions. Designed for efficient functionalization in medicinal chemistry applications.
1-[(Tert-butoxy)carbonyl]-3-cyanoazetidine-3-carboxylic acid serves as a versatile building block for the synthesis of azetidinyl scaffolds in medicinal chemistry. The tert-butyl ester provides bench stability and facilitates orthogonal deprotection, while the cyano group enables downstream functionalization via nucleophilic addition or cyclization. Its compatibility with standard coupling reactions and ease of purification make it suitable for iterative synthesis of complex heterocycles and peptide-like architectures.
|
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: