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 74003-55-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3,4-Dibromobenzaldehyde features a dibrominated aromatic ring flanking an aldehyde group, delivering enhanced electrophilicity and stability for cross-coupling reactions. This bench-stable reagent integrates efficiently into synthetic sequences requiring halogenated aryl building blocks, particularly in the construction of complex pharmaceutical intermediates and functional materials.
3,4-Dibromobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to brominated aromatic scaffolds via cross-coupling and electrophilic substitution reactions. Its dual bromine substituents provide orthogonal reactivity for sequential functionalization, while the aldehyde group facilitates condensation, reduction, or heterocycle formation. The compound exhibits good bench stability and is readily purified by crystallization, making it well-suited for use in medicinal chemistry campaigns and process development workflows.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: