23308-43-2 Usage
Chemical structure
A triamine compound consisting of three 4-N,N-dimethylaminophenyl groups attached to an ethane backbone.
Physical state
Likely a solid at room temperature, based on its molecular weight and structure.
Appearance
Unknown, but may be a colorless to pale-colored solid.
Solubility
Likely soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), but insoluble in water due to the presence of nonpolar groups.
Fluorescent properties
Used as a fluorescent dye for imaging biological structures and processes.
Applications in biology
Potential use in medical imaging, such as visualizing lymphatic vessels and detecting cancer cells.
Applications in chemistry
Used as a reagent in chemical synthesis.
Applications in materials science
Investigated for use in organic electronics and as a sensitizer in dye-sensitized solar cells.
Potential for further research
Due to its unique structure and properties, 1,1,1-TRIS(4-N,N-DIMETHYLAMINOPHENYL)-ETHANE may have additional applications in various fields, warranting further investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 23308-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,0 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23308-43:
(7*2)+(6*3)+(5*3)+(4*0)+(3*8)+(2*4)+(1*3)=82
82 % 10 = 2
So 23308-43-2 is a valid CAS Registry Number.
23308-43-2Relevant articles and documents
Photochemistry and photophysics of triarylmethane dye leuconitriles
Jarikov,Neckers
, p. 659 - 671 (2007/10/03)
The photochemical reactions of crystal violet leuconitrile (CVCN) were investigated by the means of product analysis and trapping experiments, laser flash and steady-state photolysis, and steady-state fluorescence. The influence of oxygen on the reaction was examined in detail. The photochemistry of malachite green leuconitrile (MGCN), basic fuchsin leuconitrile (BFCN), and crystal violet leucomethyl (CVMe) and leucobenzyl (CVBn), as well as triphenylacetonitrile, was studied. The results suggest ionization occurs from S1, while the di-π-methane reaction is the photochemical route from T1.
