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 7471-03-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Aminobenzo[d]thiazol-4-ol features a fused benzothiazole core with strategically positioned amino and hydroxyl groups, enabling strong hydrogen bonding and enhanced solubility. This scaffold integrates readily into bioactive molecule design, particularly in kinase inhibitors and fluorescent probes. The compound exhibits robust stability under standard bench conditions and facilitates efficient derivatization via nucleophilic substitution or coupling reactions.
2-Aminobenzo[d]thiazol-4-ol serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through straightforward derivatization at the amino and hydroxyl groups. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to pharmaceutical scaffolds, particularly in kinase inhibitor and antimicrobial agent development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H319
|
|
|
Precautionary Statements : P264-P270-P280-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: