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 61995-20-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Benzyl 3-oxopiperidine-1-carboxylate features a carbamate-protected piperidine scaffold with a ketone at the 3-position, enabling direct functionalization in synthetic routes. This bench-stable intermediate integrates readily into complex heterocyclic systems and serves as a key building block for bioactive molecule synthesis.
Benzyl 3-oxopiperidine-1-carboxylate serves as a versatile scaffold for the synthesis of piperidine-based heterocycles, enabling efficient access to medicinally relevant core structures. The ketone functionality at C3 supports selective reduction, alkylation, and enolate chemistry, while the benzyl ester permits mild deprotection under hydrogenolysis conditions. This stability and functional group compatibility make it a practical building block in medicinal chemistry workflows.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: