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 13338-49-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This imidazole derivative features a chloromethyl group enabling efficient functionalization in synthetic workflows. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating use in medicinal chemistry and peptide conjugation.
2-(Chloromethyl)-4,5-dihydro-1H-imidazole hydrochloride serves as a versatile building block for the synthesis of imidazole-containing scaffolds. Its chloromethyl group enables efficient nucleophilic substitution reactions, facilitating the construction of functionalized heterocycles. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for medicinal chemistry campaigns and process-scale applications requiring reliable reactivity and straightforward purification.
|
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: