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 5767-35-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-6-hydrazinylpyrimidine delivers a reactive hydrazino handle for conjugation chemistry, featuring a chloropyrimidine moiety that enables selective coupling under mild conditions. This bench-stable compound integrates readily into bioconjugates and functional materials, offering high reactivity with carbonyl groups and compatibility across diverse synthetic workflows.
4-Chloro-6-hydrazinylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and condensation reactions. The hydrazinyl group facilitates rapid cyclization with carbonyl-containing intermediates, while the chloro substituent provides a reliable handle for further functionalization via cross-coupling or displacement. Its bench-stable nature and compatibility with diverse reaction conditions make it valuable for medicinal chemistry campaigns and API intermediate development.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H311-H331
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: