38580-43-7 Usage
Molecular structure
A complex structure with three silicon atoms bonded to organic groups, including six methyl groups and three naphthalen-1-yl groups.
Class of compounds
Organosilicon compounds, characterized by the presence of silicon atoms bonded to organic groups.
Trisilane derivative
The compound is a derivative of trisilane, which is a type of organosilicon compound.
Industrial applications
Wide range of uses, including adhesives, sealants, and coatings in the construction and automotive industries.
Silicone polymer production
Utilized in the production of silicone polymers, which have various applications in the medical, electronics, and personal care industries.
Intermediates in organic synthesis
Serves as an intermediate in organic synthesis, which is the process of creating new organic compounds from simpler ones.
Research and potential applications
The unique structure and properties of the compound make it an interesting target for further research and potential applications in various fields.
Molecular weight
The molecular weight of the compound can be calculated based on the atomic weights of carbon (12.01 g/mol), hydrogen (1.008 g/mol), and silicon (28.085 g/mol). The molecular weight is approximately 540.93 g/mol.
Physical properties
The compound is likely to be a solid at room temperature, given its large molecular size and complexity. Further research would be needed to determine its exact physical properties, such as melting point, boiling point, and solubility.
Check Digit Verification of cas no
The CAS Registry Mumber 38580-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,8 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38580-43:
(7*3)+(6*8)+(5*5)+(4*8)+(3*0)+(2*4)+(1*3)=137
137 % 10 = 7
So 38580-43-7 is a valid CAS Registry Number.
38580-43-7Relevant articles and documents
Time-resolved fluorescence of α,ω-di(1-naphthyl)oligosilanes and 1-naphthyloligosilanes: Intramolecular excimer formation and charge-transfer interactions
Karatsu, Takashi,Nakamura, Takashi,Terasawa, Masato,Yagai, Shiki,Kitamura, Akihide,Nishimura, Yoshinobu,Yamazaki, Iwao
, p. 347 - 357 (2013/02/25)
The intramolecular photochemical processes excimer formation and charge-transfer (CT) complex formation were investigated by comparing the behavior of α,ω-di(1-naphthyl)permethyloligosilanes ((1-naphthyl)-(SiMe2) n -(1-naphthyl); NS n N, n = 1, 3, and 6) and 1-(1-naphthyl)permethyloligosilanes ((1-naphthyl)-(SiMe2) n -Me; NS n, n = 1, 3, and 6) by use of stationary and time-resolved fluorescence (TR-FL) measurements. Formation of excimer and CT complexes is highly dependent on the silicon chain length and polarity of the medium. Graphical Abstract: Intramolecular excimer formation between the two naphthyl groups and charge transfer interactions between the naphthyl and silane moieties were investigated by use of a time-correlated single-photon counting method.[Figure not available: see fulltext.]
?-? and ?-? Interactions in α,ω-Dinaphthyl and -Dianthryl Oligosilanes in Solution
Karatsu, Takashi,Shibata, Toshifumi,Nishigaki, Atsuko,Fukui, Keijiro,Kitamura, Akihide
, p. 994 - 995 (2007/10/03)
The ?-? and ?-? interactions in α,ω-1-naphthyl and di-9-anthryl oligosilanes [Np-(SiMe2)n-Np (1-4), Ant-(SiMe2)n-Ant (5-8), n=1-4] were investigated in solution. In nonpolar solvents such as cyclohexane, a strong excimer fluorescence is observed, which indicates a strong ?-? interaction. In polar solvent (CH3CN), a charge-transfer (CT) emission is observed for 3 and 4 due to the ?-? interaction.
