1079889-34-1

Basic information

• Product Name: C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)
• Synonyms: C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)
• CAS NO: 1079889-34-1
• Molecular Weight: 607.103
• Mol File: 1079889-34-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)(1079889-34-1)
• EPA Substance Registry System: C₃₃H₃₅N₂O₇⁽¹⁺⁾*Cl^(1-)(1079889-34-1)

Safety Data

• Hazardous Substances Data: 1079889-34-1(Hazardous Substances Data)

Upstream product

• 131-55-5 2,2',4,4'-tetrahydroxybenzophenone 
• 1214-24-0 3,6-dihydroxy-xanthen-9-one 
• 872516-76-2 9-oxo-9H-xanthene-3,6-diyl bis(trifluoromethanesulfonate) 
• 1023903-94-7 3,6-di(piperidin-1-yl)-9H-xanthen-9-one 
• 1174713-27-9 C₃₁H₃₅N₂O₃⁽¹⁺⁾*Cl^(1-) 
• 1079889-32-9 C₂₉H₃₁N₂O₃⁽¹⁺⁾*Cl^(1-) 

Relevant articles and documents

NOVEL PROBES AND TARGETING COMOUNDS FOR MITOCHONDRIA

The present invention provides novel compounds which are fluorescent and target the mitochondria and methods of using them.

Synthesis and spectroscopic properties of rosamines with cyclic amine substituents

(Chemical Equation Presented) There is a close structural similarity between rosamines A and rhodamines B, yet a diversity of structures in the rosamine class and their spectral properties have yet to be explored in depth. This manuscript describes a concise, scalable, solution-phase method to obtain rosamines 1-5 and 12-15, which include some water-soluble derivatives. In one test case (for 15) an illustrative protein conjugate was also formed. Throughout these products were isolated and purified, and the syntheses were found to be scalable. Further, the rosamines with these cyclic amine substituents display solvent-dependent fluorescence intensities, and high quantum yields in chlorinated hydrocarbons. In some cases the nature of the cyclic amine substituent was shown to modulate the fluorescence of the parent molecules in pH-dependent ways. The ring size of those amine substituents also correlated with some of their spectroscopic properties. Several water-soluble rosamines were prepared from some of the addition products 1-5, and one of these, 15, was efficiently conjugated to avidin via an amide linkage. The spectroscopic properties of 15 and 15-avidin in aqueous media were very similar.