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 615-20-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chlorobenzothiazole was used in the synthesis of:(RS)- and (S)-lubeluzole(1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives4H-thieno[2,3:4,5]pyrimido[2,1-b]benzothiazole derivatives
2-Chlorobenzothiazole serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted benzothiazoles via palladium-catalyzed cross-coupling reactions. Its electrophilic chlorine atom facilitates nucleophilic substitution under mild conditions, offering reliable functionalization for pharmaceutical and agrochemical scaffolds. The compound exhibits excellent bench stability and compatibility with common protecting groups, simplifying purification and scale-up in synthetic workflows.
|
GHS Pictogram :
|
GHS No : GHS06,GHS09
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅱ
|
|
Hazard Statements : H301-H319-H330-H401-H411
|
|
|
Precautionary Statements : P260-P264-P270-P271-P273-P280-P284-P305+P351+P338-P391-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: