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 208772-42-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-(tert-Butoxycarbonyl)-1H-indole-6-carboxylic acid features a bench-stable, moisture-tolerant Boc-protected indole scaffold with a carboxylic acid handle at the 6-position. This orthogonal functionality enables direct coupling in peptide and macrocycle synthesis, facilitating access to complex heterocyclic architectures under standard conditions.
1-(tert-Butoxycarbonyl)-1H-indole-6-carboxylic acid serves as a versatile building block for the synthesis of indole-based pharmaceuticals and functional materials. The Boc-protected indole scaffold enables selective deprotection and downstream coupling reactions, while the carboxylic acid functionality facilitates amide bond formation and conjugation strategies. Its bench-stable nature and compatibility with standard peptide coupling protocols make it ideal for iterative synthetic workflows in medicinal chemistry and process development.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: