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 22304-67-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4,6-Dihydroxy-5-methylisophthalaldehyde features a uniquely functionalized aromatic core with two hydroxyl groups and one methyl substituent flanking an aldehyde moiety. This configuration enables selective conjugation in bioconjugation workflows and facilitates integration into dynamic covalent architectures. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions.
4,6-Dihydroxy-5-methylisophthalaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of complex heterocyclic scaffolds and functionalized aromatic systems. Its ortho-diol and aldehyde functionalities offer complementary reactivity for selective protection, cyclization, and coupling reactions, with demonstrated utility in medicinal chemistry and materials synthesis. The methyl group enhances metabolic stability and modulates electronic properties. This compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for multi-step syntheses and scale-up applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: