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 20605-40-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Benzothiohydrazide features a reactive thiohydrazide moiety flanked by an aromatic benzene ring, enabling efficient coordination in metal complexes and integration into bioactive heterocycles. This bench-stable compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, offering high functional group tolerance and straightforward derivatization under standard conditions.
Benzothiohydrazide serves as a versatile building block in heterocyclic synthesis, enabling the construction of thiazole- and benzothiazole-containing scaffolds through cyclization with α,β-unsaturated carbonyl compounds or halogenated precursors. Its thiocarbonyl and hydrazide functionalities exhibit robust reactivity under mild conditions, facilitating efficient one-pot transformations. The compound demonstrates excellent bench stability and ease of purification, making it well-suited for iterative medicinal chemistry campaigns and process-scale applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H312-H315-H319-H332-H335
|
|
|
Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: