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 110763-40-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral thiol-containing amino acid derivative features a protected amine and a reactive sulfhydryl group, enabling selective conjugation in peptide synthesis. The tert-butyl carbamate moiety ensures stability during handling and purification, while the mercapto functionality facilitates site-specific labeling or disulfide bridge formation in bioconjugation workflows.
(R)-2-((tert-Butoxycarbonyl)amino)-3-mercapto-3-methylbutanoic acid serves as a versatile chiral building block for the synthesis of cysteine-derived peptidomimetics and thioether-containing heterocycles. The protected amine and free thiol functionalities enable orthogonal transformations, while the tert-butyl carbamate group provides bench stability and facile deprotection under mild acidic conditions. This scaffold is well-suited for solid-phase synthesis and conjugation chemistry in medicinal chemistry campaigns.
|
GHS Pictogram :
|
GHS No : GHS07,GHS08,GHS09
|
|
Signal Word : Danger
|
UN#: 3077
|
|
Class : 9
|
Packing Group : Ⅲ
|
|
Hazard Statements : H315-H319-H372-H413
|
|
|
Precautionary Statements : P264-P273-P280-P302+P352-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: