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 3096-70-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Amino-3,5-dimethylphenol features a phenolic hydroxyl group flanked by two methyl substituents and an amino functionality at the para position relative to the hydroxyl. This electron-rich scaffold enables direct incorporation into conjugated systems and facilitates metal-catalyzed coupling reactions. The compound exhibits enhanced solubility in organic solvents and stability under standard bench conditions, making it suitable for synthetic intermediates in pharmaceutical and materials chemistry.
4-Amino-3,5-dimethylphenol serves as a versatile building block in synthetic organic chemistry, enabling the construction of substituted anilines and heterocyclic scaffolds. Its ortho-dimethyl substitution enhances stability and facilitates selective functionalization, while the amino and phenolic groups offer complementary reactivity for coupling reactions and derivatization. This compound is bench-stable and amenable to purification via recrystallization, making it well-suited for use in medicinal chemistry campaigns and process development.
|
GHS Pictogram :
|
GHS No : GHS09
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H400
|
|
|
Precautionary Statements : P273-P391-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: