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 33769-07-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This trityl-protected imidazole derivative serves as a robust scaffold for nucleoside and oligonucleotide synthesis. The bulky trityl group confers exceptional stability during purification and handling, while the methanol-functionalized imidazolyl moiety enables efficient coupling reactions under standard conditions. Designed for high-yield incorporation in sensitive synthetic sequences, this compound delivers reliable protection and orthogonal reactivity.
(1-Trityl-1H-imidazol-4-yl)methanol serves as a robust protecting group strategy for imidazole nucleophiles, enabling selective functionalization in complex molecule synthesis. The trityl moiety provides excellent stability under diverse reaction conditions, facilitates easy purification by precipitation, and can be removed cleanly under mild acidic conditions. This compound functions as a key building block in the construction of heterocyclic scaffolds and peptide conjugates, offering high functional group tolerance and compatibility with standard synthetic 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-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: