1260119-25-2
1260119-25-2
Chemical Structure
Boc-L-Cys(Propargyl)-OH
- CAS No.: 1260119-25-2
- Formula:C11H17NO4S
- Molecular Weight:259.32
IUPAC Name: N-(tert-butoxycarbonyl)-S-(prop-2-yn-1-yl)-L-cysteine
InChIKey: MSLYNMSPLZOMMP-QMMMGPOBSA-N
SMILES: CC(C)(C)OC(N[C@H](C(O)=O)CSCC#C)=O
Biological Activity: Boc-L-Cys(Propargyl)-OH is a click chemistry reagent. Boc-L-Cys(Propargyl)-OH can be used for the research of various biochemical[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Boc-L-Cys(Propargyl)-OH | Boc-L-Cys(Propargyl)-OH is a click chemistry reagent. Boc-L-Cys(Propargyl)-OH can be used for the research of various biochemical. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Mauro Lo Conte, et al. Photoinduced addition of glycosyl thiols to alkynyl peptides: use of free-radical thiol-yne coupling for post-translational double-glycosylation of peptides. [Content Brief]
- [2]. Charlotte Collet, et al. Development of 6-[(18) F]fluoro-carbohydrate-based prosthetic groups and their conjugation to peptides via click chemistry. J Labelled Comp Radiopharm. 2016 Feb;59(2):54-62. [Content Brief]
Keywords
