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 141940-32-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid derivative features a tert-butoxycarbonyl-protected amine and a fluorinated aromatic ring, enabling stable incorporation into peptide conjugates. The para-fluorine enhances metabolic resistance, while the carboxylic acid facilitates coupling reactions under standard conditions.
5-[(tert-Butoxycarbonyl)amino]-2-fluorobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated aromatic scaffolds. The ortho-fluoro group facilitates directed metalation and subsequent functionalization, while the tert-butoxycarbonyl (Boc) amine and carboxylic acid functionalities offer orthogonal reactivity for peptide coupling and selective deprotection. Its bench-stable nature and compatibility with standard protecting group strategies make it well-suited for multi-step syntheses of bioactive molecules.
|
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: