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 1314738-42-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This cyclopropanecarboxylic acid derivative features a para-chloroaniline moiety linked via a cyclopropyl bridge, delivering enhanced metabolic stability and targeted bioactivity. The electron-rich aromatic ring enables efficient coupling in medicinal chemistry workflows, while the carboxylic acid group facilitates conjugation or salt formation. Bench-stable and moisture-tolerant, it serves as a key scaffold for kinase inhibitor development and peptide-based drug discovery.
1-(4-Amino-3-chlorophenyl)cyclopropanecarboxylic acid serves as a versatile building block for medicinal chemistry campaigns, enabling direct incorporation into bioactive scaffolds via amide coupling or decarboxylation. The cyclopropane ring imparts conformational rigidity, while the amino and chloro substituents offer orthogonal handles for further functionalization. Bench-stable and readily purified by crystallization, it facilitates scalable synthesis of targeted compounds in drug discovery workflows.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: