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 52448-17-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-L-tryptophan integrates a bromine substituent at the indole C6 position, enabling site-specific functionalization in peptide synthesis and chemical biology applications. This bench-stable, moisture-tolerant derivative retains the native amino acid scaffold for seamless incorporation into biologically active sequences.
6-Bromo-L-tryptophan serves as a valuable building block for the synthesis of brominated indole derivatives and peptidomimetics. Its well-defined functionalization at the 6-position enables site-specific modifications in medicinal chemistry campaigns, while maintaining compatibility with standard peptide coupling protocols. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it ideal for use in multi-step synthetic sequences targeting heterocyclic scaffolds and bioactive compounds.
|
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: