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 6502-22-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Isopropylbenzaldehyde features a para-substituted aromatic ring with an isopropyl group flanking a reactive aldehyde moiety. This electron-rich scaffold enables direct integration into Suzuki-Miyaura couplings and reductive amination workflows under standard conditions. The sterically hindered isopropyl substituent enhances regioselectivity in electrophilic aromatic substitution reactions.
2-Isopropylbenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized aromatic scaffolds. Its aldehyde functionality facilitates standard transformations including nucleophilic additions, reductive amination, and condensation reactions. The ortho-isopropyl group provides steric and electronic modulation, enhancing regioselectivity in electrophilic substitutions and improving bench stability for handling and purification. This compound functions effectively in the synthesis of pharmaceutical intermediates and agrochemicals requiring substituted benzaldehyde motifs.
|
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-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: