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 72235-52-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Difluorobenzylamine has been used in the synthesis of AlaAib(N-fluoroarylmethyl)], nonpolar nucleobase dipeptide via Ugi four-component condensation reaction.
(2,4-Difluorophenyl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive scaffolds through standard amine coupling and electrophilic substitution reactions. Its fluorinated aryl core enhances metabolic stability and modulates electronic properties, while the primary amine facilitates conjugation with carboxylic acids, sulfonyl chlorides, and isocyanates. Bench-stable and readily purified by distillation or chromatography, it functions reliably in multi-step syntheses of pharmaceutical intermediates and functional materials.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 2735
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: