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 4492-02-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate is a bench-stable heterocyclic ester featuring a saturated indazole core with a carboxylate handle. This scaffold integrates readily into synthetic sequences requiring nitrogen-rich, electron-deficient platforms. The ester group enables straightforward derivatization under standard conditions.
Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to indazole-based scaffolds. The tetrahydroindazole core offers enhanced solubility and metabolic stability compared to its aromatic counterpart, while the ester functionality facilitates downstream transformations such as hydrolysis, amidation, or coupling reactions. Its bench-stable nature and compatibility with standard cross-coupling and reductive amination protocols make it a practical choice for synthesizing biologically active molecules and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: