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 65003-40-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This benzodiazole derivative features a strategically positioned methoxycarbonyl-amino group flanked by a carboxylic acid, enabling direct conjugation and solubility enhancement. The scaffold integrates robust stability with orthogonal functional handles, facilitating efficient incorporation into peptide-based systems and bioconjugation workflows under standard conditions.
2-[(Methoxycarbonyl)amino]-1H-1,3-benzodiazole-6-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted benzodiazole scaffolds. Its dual functionality—carboxylic acid and ester-amide groups—facilitates orthogonal transformations in peptide coupling, cyclization, and conjugation workflows. The compound exhibits excellent bench stability and simplifies purification, making it well-suited for medicinal chemistry campaigns and API intermediate development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: