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 6201-65-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chlororesorcinol features a chlorinated aromatic ring system with three hydroxyl groups, offering enhanced reactivity in electrophilic substitution and serving as a key intermediate in dye synthesis. The ortho-chloro substituent imparts electron-withdrawing character, stabilizing reaction intermediates under standard conditions. This bench-stable compound integrates readily into complex molecular architectures requiring precise functional group placement.
2-Chlororesorcinol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds. Its ortho-chloro and dihydroxy functionalities facilitate electrophilic substitution, Suzuki-Miyaura coupling, and directed metalation reactions. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it suitable for iterative synthesis of bioactive heterocycles and functionalized aromatics in medicinal chemistry 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: