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 1259223-99-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This cyclobutyl-substituted benzoic acid features a tert-butoxycarbonyl-protected amine, enabling straightforward incorporation into peptide synthesis. The rigid cyclobutyl ring imparts conformational stability, while the carboxylic acid group facilitates coupling reactions under standard conditions.
4-(1-((tert-Butoxycarbonyl)amino)cyclobutyl)benzoic acid serves as a versatile building block for medicinal chemistry and peptide conjugation, enabling the synthesis of cyclobutyl-containing bioactive molecules. The tert-butyl carbamate (Boc) group provides excellent stability during synthetic manipulations and can be selectively removed under mild acidic conditions. The carboxylic acid functionality facilitates coupling reactions with amines or alcohols, while the cyclobutyl ring imparts conformational rigidity beneficial for structure-activity studies.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: