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 201338-62-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This methyl ester of 2-[bis[(1,1-dimethylethoxy)carbonyl]amino]-2-propenoic acid features a sterically hindered carbamate-protected amine group flanked by an electron-deficient enoate system. The di-tert-butoxycarbonyl (DTB) moiety provides exceptional bench stability and moisture tolerance, enabling straightforward handling in synthetic workflows. This protected aminoacrylate derivative integrates readily into peptide-like architectures and serves as a key building block for conjugation strategies requiring orthogonal deprotection.
2-[Bis[(1,1-dimethylethoxy)carbonyl]amino]-2-propenoic acid methyl ester serves as a stable, bench-ready building block for peptide synthesis and heterocyclic scaffolds. Its tert-butoxycarbonyl (Boc) groups provide robust protection of amine functionalities, enabling orthogonal deprotection in standard workflows. The acrylate moiety facilitates conjugate addition reactions and serves as a versatile handle for Michael-type additions or polymerization. Designed for ease of handling and purification, it supports scalable synthesis and is compatible with common reaction conditions in medicinal chemistry and process development.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: