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 223562-52-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-(Prop-1-yn-1-yl)benzoic acid features a propargyl group attached to the para position of a benzoic acid scaffold, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC). This alkyne functionality integrates readily into bioconjugation workflows and modular synthesis, offering high chemoselectivity under mild conditions.
4-(Prop-1-yn-1-yl)benzoic acid serves as a versatile synthetic building block for alkyne-functionalized aromatic systems. The terminal alkyne group enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid access to triazole-linked scaffolds. Its benzoic acid functionality supports direct derivatization via amide or ester formation, offering orthogonal reactivity for modular synthesis. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for applications in medicinal chemistry and materials science.
|
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: