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 60710-39-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromo-4-methylphenol features a bromine atom at the meta position relative to a hydroxyl group, paired with a methyl substituent at the para position. This arrangement imparts enhanced reactivity in cross-coupling processes while maintaining stability under standard bench conditions. The compound serves as a key intermediate in synthesizing functionalized aromatic scaffolds for pharmaceutical and agrochemical development.
3-Bromo-4-methylphenol serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted aromatic scaffolds. Its bromine and phenolic hydroxyl groups provide orthogonal reactivity for palladium-catalyzed cross-coupling and electrophilic functionalization. The methyl group enhances solubility and influences regioselectivity in downstream transformations. Bench-stable and readily purified by recrystallization, it functions reliably in medicinal chemistry and materials synthesis 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: