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 104-11-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-N-methylbenzylamine features a para-chlorinated benzyl scaffold with a tertiary amine handle, enabling direct incorporation into pharmaceutical intermediates. The electron-withdrawing chlorine substituent enhances electrophilic reactivity at the aromatic ring while the N-methyl group improves metabolic stability and solubility in organic media. This bifunctional architecture supports efficient coupling reactions under mild conditions.
4-Chloro-N-methylbenzylamine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its benzylic amine functionality exhibits excellent reactivity in coupling and cyclization reactions, while the ortho-chloro substituent provides a handle for further derivatization via palladium-catalyzed cross-coupling. The N-methyl group enhances metabolic stability and modulates basicity, improving membrane permeability. Bench-stable and readily purified by distillation or chromatography, it functions efficiently in standard synthetic workflows.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 2735
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314-H318
|
|
|
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: