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 18437-66-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl 4-chlorophenylcarbamate serves as a robust protecting group for primary amines, offering stability under basic conditions and facilitating straightforward deprotection. The para-chlorophenyl moiety enhances solubility in organic solvents, while the tert-butyl carbamate fragment ensures compatibility with diverse synthetic workflows. This derivative integrates cleanly into peptide synthesis and small-molecule drug discovery.
tert-Butyl 4-chlorophenylcarbamate serves as a stable, bench-ready carbamate protecting group for primary amines, enabling selective amidation and coupling reactions in peptide and heterocycle synthesis. Its chlorine substituent enhances electrophilic reactivity in palladium-catalyzed cross-coupling processes, facilitating efficient C–N bond formation. The tert-butyl moiety ensures straightforward deprotection under mild acidic conditions, preserving sensitive functional groups.
|
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: