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 183062-96-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This azetidine-based acetic acid derivative features a tert-butoxycarbonyl-protected amine, enabling straightforward functionalization in peptide synthesis. The strained azetidinyl ring imparts enhanced reactivity and metabolic stability, while the carboxylic acid group facilitates conjugation or derivatization under standard conditions.
2-(1-(tert-Butoxycarbonyl)azetidin-3-yl)acetic acid serves as a versatile building block for the synthesis of bioactive azetidine-containing compounds. The tert-butoxycarbonyl (Boc) group provides stable protection of the amine, enabling orthogonal manipulation in multi-step sequences. The acetic acid side chain facilitates conjugation via amide bond formation or further functionalization, while the strained azetidine ring imparts unique conformational rigidity. This compound exhibits excellent bench stability and compatibility with standard purification techniques, making it well-suited for medicinal chemistry campaigns targeting kinase inhibitors, CNS agents, and other therapeutically relevant scaffolds.
|
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: