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 2533-69-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2,2,2-trichloroacetimidate was used as starting material during the synthesis of novel bibenzimidazole oligomers and polymers. It was employed as reagent during the synthesis of 2,2-bisbenzimidazole-5,5-dicarboxylic acid.
2,2,2-Trichloroacetimidic acid methyl ester serves as a stable, bench-ready reagent for the efficient synthesis of N-protected imines and enamines. Its trichloromethyl group enhances electrophilicity, enabling selective reactions with amines under mild conditions. The methyl ester functionality offers ease of purification and compatibility with common workup procedures, making it a practical choice for building blocks in heterocyclic chemistry and targeted molecule synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H227-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: