1352809-04-1 Usage
Uses
Used in Photoactivatable Compounds:
Bis(4,5-dimethoxy-2-nitrobenzyl) 6-(2,4-bis(((2,4-dimethoxybenzyl)oxy)carbonyl)phenyl)-3,4,6,8,9,10-hexahydro-1Hpyrano[3,2-g:5,6-g']diquinoline-1,11(2H)-dicarboxylate is used as a photoactivatable rhodamine derivative in the field of biochemistry and molecular biology. The carboxylic acid functionality allows for conjugation to amine-containing compounds or biomolecules through amide coupling procedures, enabling the study of various biological processes.
Used in Fluorescence Restoration:
In the field of fluorescence microscopy and imaging, bis(4,5-dimethoxy-2-nitrobenzyl) 6-(2,4-bis(((2,4-dimethoxybenzyl)oxy)carbonyl)phenyl)-3,4,6,8,9,10-hexahydro-1Hpyrano[3,2-g:5,6-g']diquinoline-1,11(2H)-dicarboxylate is used for fluorescence restoration. The ortho-Nitroveratryloxycarbonyl (NVOC) cages can be removed upon irradiation with UV light, restoring the fluorescence of the base dye. This property makes it a valuable tool for controlling the fluorescence of labeled biomolecules in living cells or tissues.
Used in Drug Delivery Systems:
Similar to gallotannin, bis(4,5-dimethoxy-2-nitrobenzyl) 6-(2,4-bis(((2,4-dimethoxybenzyl)oxy)carbonyl)phenyl)-3,4,6,8,9,10-hexahydro-1Hpyrano[3,2-g:5,6-g']diquinoline-1,11(2H)-dicarboxylate can be employed in drug delivery systems to improve the delivery, bioavailability, and therapeutic outcomes of various drugs. The compound's ability to form conjugates with amine-containing compounds can be utilized to develop novel drug delivery systems, such as organic and metallic nanoparticles, for targeted drug delivery.
Used in Pharmaceutical Research:
Due to its unique chemical structure and photoactivatable properties, bis(4,5-dimethoxy-2-nitrobenzyl) 6-(2,4-bis(((2,4-dimethoxybenzyl)oxy)carbonyl)phenyl)-3,4,6,8,9,10-hexahydro-1Hpyrano[3,2-g:5,6-g']diquinoline-1,11(2H)-dicarboxylate has potential applications in pharmaceutical research. It can be used as a starting material for the development of new drugs or as a tool to study the interactions between drugs and their target molecules.
Used in Chemical Synthesis:
In the field of organic chemistry, bis(4,5-dimethoxy-2-nitrobenzyl) 6-(2,4-bis(((2,4-dimethoxybenzyl)oxy)carbonyl)phenyl)-3,4,6,8,9,10-hexahydro-1Hpyrano[3,2-g:5,6-g']diquinoline-1,11(2H)-dicarboxylate can be used as a building block or intermediate in the synthesis of more complex molecules. Its unique structure and functional groups can be exploited to create new compounds with potential applications in various industries, such as pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1352809-04-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,8,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1352809-04:
(9*1)+(8*3)+(7*5)+(6*2)+(5*8)+(4*0)+(3*9)+(2*0)+(1*4)=151
151 % 10 = 1
So 1352809-04-1 is a valid CAS Registry Number.
1352809-04-1Relevant academic research and scientific papers
Facile and general synthesis of photoactivatable xanthene dyes
Wysocki, Laura M.,Grimm, Jonathan B.,Tkachuk, Ariana N.,Brown, Timothy A.,Betzig, Eric,Lavis, Luke D.
supporting information; experimental part, p. 11206 - 11209 (2012/02/03)
Despite the apparent simplicity of the xanthene fluorophores, the preparation of caged derivatives with free carboxy groups remains a synthetic challenge. A straightforward and flexible strategy for preparing rhodamine and fluorescein derivatives was developed using reduced, "leuco" intermediates. Copyright
