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 159635-22-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl 3-hydroxy-4-methylidenepiperidine-1-carboxylate features a rigid piperidine core with a strategically positioned hydroxyl group and exocyclic methylene moiety, enabling direct functionalization at C3 and C4. This scaffold supports efficient access to complex nitrogen heterocycles in medicinal chemistry and natural product synthesis.
tert-Butyl 3-hydroxy-4-methylidenepiperidine-1-carboxylate serves as a versatile scaffold for the synthesis of piperidine-based heterocycles, enabling efficient access to medicinally relevant frameworks. The pendant hydroxyl group facilitates selective derivatization, while the exocyclic methylene moiety supports Diels–Alder reactions and Michael additions. Its tert-butyl carbamate protection offers excellent bench stability and ease of deprotection under mild acidic conditions, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
|
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: