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 219508-62-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Boc-6-amino-indole features a protected amine at the 6-position of the indole scaffold, enabling stable incorporation into peptide and heterocyclic syntheses. The Boc group ensures compatibility with standard deprotection protocols while maintaining solubility under routine reaction conditions. This derivative serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and bioactive natural product analogs.
1-Boc-6-amino-indole serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds. The Boc group provides excellent stability and orthogonal protection for the amine, facilitating subsequent functionalization via standard deprotection and coupling reactions. Its compatibility with diverse reaction conditions supports its use in peptide conjugation, heterocycle synthesis, and late-stage derivatization within multi-step synthetic sequences.
|
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: