1100365-01-2

Basic information

• Product Name: N-(6-(diethylamino)-9-(2-(piperazine-1-carbonyl)phenyl)-3H-xanthen-3-ylidene)-N-ethylethanaminium 2,2,2-trifluoroacetate
• Synonyms: N-(6-(diethylamino)-9-(2-(piperazine-1-carbonyl)phenyl)-3H-xanthen-3-ylidene)-N-ethylethanaminium 2,2,2-trifluoroacetate
• CAS NO: 1100365-01-2
• Molecular Weight: 624.703
• Mol File: 1100365-01-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(6-(diethylamino)-9-(2-(piperazine-1-carbonyl)phenyl)-3H-xanthen-3-ylidene)-N-ethylethanaminium 2,2,2-trifluoroacetate(CAS DataBase Reference)
• NIST Chemistry Reference: N-(6-(diethylamino)-9-(2-(piperazine-1-carbonyl)phenyl)-3H-xanthen-3-ylidene)-N-ethylethanaminium 2,2,2-trifluoroacetate(1100365-01-2)
• EPA Substance Registry System: N-(6-(diethylamino)-9-(2-(piperazine-1-carbonyl)phenyl)-3H-xanthen-3-ylidene)-N-ethylethanaminium 2,2,2-trifluoroacetate(1100365-01-2)

Safety Data

• Hazardous Substances Data: 1100365-01-2(Hazardous Substances Data)

Upstream product

• 110-85-0 piperazine 
• 509-34-2 rhodamine B 
• 76-05-1 trifluoroacetic acid 

Relevant articles and documents

Synthesis of a toolbox of clickable rhodamine B derivatives

Abstract An efficient method for the large-scale preparation of rhodamine B clickable derivatives has been developed. Starting from inexpensive rhodamine B as the starting material it was possible to functionalize the carboxylic functionality of rhodamine B with an azide, a strained-alkyne, a substituted triphenylphosphine, a thiol, and a maleimide. Through the synthetic strategy it was possible to obtain stable and pure clickable rhodamine compounds that can be readily used not only for chemoselectively probing biomolecules, but also for materials science.

Ratiometric fluorescence detection of pathogenic bacteria resistant to broad-spectrum β-lactam antibiotics

Identification of bacteria: A methoxyimino cephalosporin derivative containing a pair of fluorescence resonance energy transfer (FRET) fluorophores was synthesized. This probe displays selective cleavage toward different types of β-lactamases, thereby pro