65303-14-2 Usage
Molecular structure
The compound consists of two benzthiazolium groups connected to each other through a cyclopentenyl structure, with a chloro and ethyl group attached.
Iodide ion
The compound is bound to an iodide ion.
Physical properties
The compound is a yellow-orange dye.
Biological applications
The compound is used in biological staining, fluorescence microscopy, and as a vital stain in cell culture.
Cellular processes
The compound is used as a probe for detecting lipid rafts in cell membranes and as a marker for apoptosis.
Technological applications
The compound has potential applications in the field of organic electronic materials and photovoltaic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 65303-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,0 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65303-14:
(7*6)+(6*5)+(5*3)+(4*0)+(3*3)+(2*1)+(1*4)=102
102 % 10 = 2
So 65303-14-2 is a valid CAS Registry Number.
65303-14-2Relevant academic research and scientific papers
CHEMISTRY OF ENOL ETHERS. LII. REACTION OF THE VINYLOGS OF THE VILSMEIER COMPLEX WITH HETEROCYCLIC COMPOUNDS AS A NEW METHOD FOR THE SYNTHESIS OF CYANINE DYES
Makin, S. M.,Pomogaev, A. I.
, p. 2020 - 2024 (2007/10/02)
During the condensation of the vinylogs of the Vilsmeier complex with quaternary salts of heterocyclic bases containing an active methyl group the meso-substituted di- and tricarbocyanine dyes are formed.
