99643-54-6 Usage
Uses
Used in Organic Electronics:
2,2-dimethylnaphtho[2,3-d][1,3]dithiole is used as a component in organic electronic devices for its electronic properties that can enhance the performance of these devices.
Used in Material Science:
In the field of material science, 2,2-dimethylnaphtho[2,3-d][1,3]dithiole is utilized as a building block for the development of new materials, leveraging its unique structure to create materials with specific properties.
Used in Pharmaceutical Research:
2,2-dimethylnaphtho[2,3-d][1,3]dithiole is employed as a molecular scaffold in pharmaceutical research for designing new drugs, due to its potential to interact with biological targets in innovative ways.
Used in Chemical Synthesis:
2,2-dimethylnaphtho[2,3-d][1,3]dithiole serves as an intermediate in the synthesis of more complex organic compounds, taking advantage of its reactive sites for further functionalization.
Used in Research and Development:
As a subject of study in research and development, 2,2-dimethylnaphtho[2,3-d][1,3]dithiole is used to explore its properties and potential applications, driving scientific discovery and technological advancement in related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 99643-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,4 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99643-54:
(7*9)+(6*9)+(5*6)+(4*4)+(3*3)+(2*5)+(1*4)=186
186 % 10 = 6
So 99643-54-6 is a valid CAS Registry Number.
99643-54-6Relevant academic research and scientific papers
Electronic Structure of Heterospirenes-PE Spectroscopic Investigations
Gleiter, Rolf,Uschmann, Joachim
, p. 370 - 380 (2007/10/02)
The synthesis of the heterospirenes 1-9 is described and their He I photoelectron (PE) spectra are recorded.The assignment of the first PE bands is based on a comparison with fragment molecules and on molecular orbital calculations using semiempirical methods (PPP, MINDO/3). in the case of 1, 2, 4, and 5 strong spirointeraction has been elucidated.For 3 the analysis of the spectrum is hampered due to the strong overlap of the bands while for 6 the nonplanarity brings about a reduction of spirointeractions.For 7-9 the interaction between both fragments could not be detected.
