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 160709-02-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This D-threo-pentitol derivative integrates a 1H-1,2,4-triazolyl group and a 2,4-difluorophenyl substituent at the C-2 position, featuring a 2,5-anhydro scaffold that enhances metabolic stability. The hydroxymethyl group at C-4 provides a handle for further derivatization. This structure combines polar functionality with fluorinated aromatic character, enabling selective interactions in glycosylation studies and bioconjugation workflows under standard conditions.
This compound serves as a versatile glycosyl donor scaffold, enabling stereoselective glycosylation reactions under mild conditions. The 1H-1,2,4-triazolyl group provides enhanced stability and facilitates purification, while the difluorophenyl and hydroxymethyl substituents offer orthogonal functional handles for downstream conjugation. Its robust bench stability and compatibility with standard synthetic protocols make it well-suited for complex oligosaccharide assembly and medicinal chemistry applications.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: