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 1164116-18-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4,6-Dichloro-2-isobutylpyrimidine features a sterically hindered isobutyl group at the 2-position, enhancing solubility and stability. The electron-deficient pyrimidine core facilitates nucleophilic substitution, enabling efficient coupling in medicinal chemistry workflows. This bench-stable reagent streamlines synthesis of functionalized heterocycles under standard conditions.
4,6-Dichloro-2-isobutylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds through nucleophilic substitution. The dichloro pattern facilitates sequential functionalization at C4 and C6 positions, while the isobutyl group provides steric and electronic modulation. Bench-stable and compatible with standard coupling protocols, it supports rapid diversification for target-oriented synthesis and process development.
|
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+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: