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 20605-01-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Reagent for preparing 1,3-dioxanes from acetals, aldehydes, and ketones.
Diethyl 2,2-bis(hydroxymethyl)malonate serves as a versatile synthon for the construction of tetrahydrofuran and pyran ring systems, enabling efficient access to oxygenated heterocyclic scaffolds. Its bis(hydroxymethyl) functionality supports orthogonal protection strategies and participates reliably in dehydration, cyclization, and coupling reactions under standard conditions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and natural product derivatization.
|
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: