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 89151-44-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
N-Boc-4-Piperidineethanol features a protected piperidine ring with a terminal hydroxymethyl group, enabling straightforward deprotection and functionalization. This bench-stable derivative integrates readily into medicinal chemistry campaigns, serving as a key scaffold for bioactive molecule synthesis.
N-Boc-4-Piperidineethanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of piperidine-containing scaffolds. The Boc-protected amine offers excellent bench stability and compatibility with standard deprotection protocols, while the terminal hydroxyl group facilitates derivatization via esterification or ether formation. Its defined stereochemistry and functional group tolerance make it ideal for modular synthesis of bioactive compounds and 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: