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 6443-69-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3,4,5-Trimethoxytoluene was used as a substructure model compound in the reaction of trimethoprim with free available chlorine (i.e. HOCl).
1,2,3-Trimethoxy-5-methylbenzene serves as a versatile aromatic building block in medicinal chemistry and agrochemical synthesis. Its three methoxy groups provide strong electron-donating effects, enhancing reactivity in electrophilic substitution reactions. The methyl group offers a site for further functionalization, while the trimethoxy pattern ensures good bench stability and solubility. This compound facilitates efficient access to complex heterocyclic scaffolds and is compatible with standard coupling protocols, making it a practical choice for iterative 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: