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 1310481-47-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates a para-substituted aryl group with a sterically hindered tert-butoxycarbonyl-protected amine, enabling selective functionalization in late-stage diversification. The pendant amine facilitates conjugation under standard conditions while the boronic acid supports Suzuki-Miyaura coupling, offering robust stability and ease of handling for complex molecule synthesis.
(4-(2-((tert-Butoxycarbonyl)amino)ethyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds with retained amine functionality. The tert-butoxycarbonyl (Boc) group provides excellent stability during reaction setup and facilitates orthogonal deprotection. This reagent exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
|
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: