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 58588-59-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Chloro-4-formylbenzoic acid features a strategically positioned formyl group adjacent to a carboxylic acid, enabling direct conjugation in coupling reactions. The electron-withdrawing chlorine substituent enhances electrophilicity at the formyl carbon, facilitating efficient nucleophilic addition. This ortho-functionalized scaffold integrates readily into bioactive molecule synthesis and serves as a key intermediate in medicinal chemistry campaigns targeting heterocyclic systems.
3-Chloro-4-formylbenzoic acid serves as a versatile building block in medicinal chemistry, enabling direct access to substituted benzimidazoles and heterocyclic scaffolds via condensation reactions. The ortho-functionalized core supports efficient derivatization through the formyl and carboxylic acid groups, offering excellent bench stability and straightforward purification. Its dual reactivity facilitates modular synthesis of bioactive molecules with high functional group tolerance.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: