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 889953-29-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-bearing benzoic acid derivative features a tert-butoxycarbonyl-protected pyrrolidine moiety, enabling stable incorporation into complex molecular architectures. The para-substituted aryl group enhances conjugation and facilitates downstream functionalization. Designed for synthetic versatility in medicinal chemistry and peptide coupling workflows, this compound offers reliable reactivity under standard conditions with minimal handling complications.
2-(1-(tert-Butoxycarbonyl)pyrrolidin-3-yl)benzoic acid serves as a versatile building block for medicinal chemistry, enabling the construction of pyrrolidine-containing heterocycles via standard deprotection and coupling reactions. The tert-butyl ester group offers bench stability and orthogonal compatibility, facilitating selective manipulation in multi-step syntheses. Its carboxylic acid functionality supports direct amide bond formation or derivatization, making it ideal for scaffold diversification in drug discovery campaigns.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: