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 212555-23-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This thiol features a (2,4,6-trimethoxyphenyl) group that enhances solubility and electron density, enabling efficient conjugation in bioconjugation workflows. The benzylic sulfhydryl moiety delivers high reactivity under mild conditions, facilitating site-specific labeling of biomolecules.
(2,4,6-Trimethoxyphenyl)methanethiol serves as a robust thiol building block in synthetic organic chemistry, enabling efficient conjugation and functionalization reactions. Its electron-rich arylthiol structure enhances reactivity in nucleophilic substitution and metal-catalyzed coupling processes. The trimethoxy substituents provide excellent bench stability and facilitate purification via chromatography or crystallization, making it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301+H311+H331-H315-H319
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: