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 19785-39-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This thiazole-acetonitrile derivative features a methyl-substituted 1,3-thiazole ring linked to a nitrile-bearing acetyl group. The electron-deficient heterocycle pairs with the polar nitrile functionality to enable selective coupling in synthetic transformations. Bench-stable and moisture-tolerant, it integrates efficiently into multistep syntheses requiring robust heterocyclic scaffolds.
2-(4-Methyl-1,3-thiazol-2-yl)acetonitrile serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its structure combines a thiazole ring with a reactive nitrile group, enabling diverse transformations including nucleophilic additions, metal-catalyzed couplings, and functionalization at the acetonitrile moiety. The molecule exhibits good bench stability and facilitates efficient synthesis of heterocyclic scaffolds and potential API intermediates.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: