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 52010-98-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-(Hydroxymethyl)benzaldehyde features a benzaldehyde core functionalized with a hydroxymethyl group at the meta position, enabling dual reactivity. This combination facilitates efficient coupling reactions and serves as a key scaffold in synthetic intermediates for pharmaceuticals and functional materials. The molecule exhibits enhanced solubility and stability under standard conditions.
3-(Hydroxymethyl)benzaldehyde serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient access to complex scaffolds through orthogonal functional group manipulation. The aldehyde group facilitates nucleophilic additions and condensation reactions, while the pendant hydroxymethyl moiety supports selective oxidation, protection, or derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for applications in medicinal chemistry, heterocycle synthesis, and molecular scaffold diversification.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H317-H319
|
|
|
Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: