17973-82-9 Usage
Uses
Used in Catalysis:
1,3-dichloro-1,1,3,3-tetraethyldistannoxane is used as a catalyst in organic synthesis reactions due to its ability to facilitate various chemical transformations, enhancing the efficiency and selectivity of these processes.
Used in Materials Science:
1,3-dichloro-1,1,3,3-tetraethyldistannoxane is utilized in materials science for its capacity to form thin films, which are essential for the development of electronic devices. The properties of these films can be tailored for specific applications, such as in semiconductors or sensors.
Used in Electronic Devices:
1,3-dichloro-1,1,3,3-tetraethyldistannoxane is used as a component in the fabrication of electronic devices, particularly for creating thin films that can be integrated into semiconductors or sensors, contributing to the performance and functionality of these devices.
However, it is important to note that due to the toxic and harmful nature of organotin compounds, the use of 1,3-dichloro-1,1,3,3-tetraethyldistannoxane is subject to limitations and regulations to ensure safety and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 17973-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,7 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17973-82:
(7*1)+(6*7)+(5*9)+(4*7)+(3*3)+(2*8)+(1*2)=149
149 % 10 = 9
So 17973-82-9 is a valid CAS Registry Number.
InChI:InChI=1/4C2H5.2ClH.H2O.2Sn/c4*1-2;;;;;/h4*1H2,2H3;2*1H;1H2;;/q;;;;;;;2*+1/p-2/r2C4H10ClSn.H2O/c2*1-3-6(5)4-2;/h2*3-4H2,1-2H3;1H2
17973-82-9Relevant academic research and scientific papers
Multinuclear 1D and 2D NMR investigations on the interaction between the pyrimidic nucleotides 5'-CMP, 5'-dCMP, and 5'-UMP and diethyltin dichloride in aqueous medium
Ghys, Laurent,Biesemans, Monique,Gielen, Marcel,Garoufis, Achilleas,Hadjiliadis, Nick,Willem, Rudolph,Martins, Jose C.
, p. 513 - 522 (2007/10/03)
The interactions between diethyltin dichloride and 5'-CMP, 5'-dCMP, and 5'-UMP in aqueous solution were investigated by multinuclear 1D and 2D NMR techniques including 119Sn, 15N and 31P nuclei. These studies were combined with electrospray mass spectrometry, infrared spectroscopy, solid state 13C, 31P and 117Sn CP-MAS NMR, and elemental analysis. As demonstrated by 31P-1H HOESY spectroscopy, the diethyltin moiety interacts with the phosphate group of the pyrimidic mononucleotides in the pH range 0.5-3.5. Compound 8 (X = Cl), the solid isolated in this pH range from 5'- CMP, contains two tin atoms bridged by one oxygen and one chlorine atom, each tin atom being linked to the phosphate group of a nucleotide moiety. For 5'- UMP the solid isolated (12) has a dimeric structure with two different tin atoms; it can be formed by dimerization of compound 11 with the elimination of two water molecules. As demonstrated by 1H-119Sn HMQC correlation NMR data and the 2J(119Sn-O-117Sn) coupling constant of 156 Hz, the diethyltin moiety reacts with the O(2') and O(3') oxygen atoms of the nucleotides to form a dimeric diethyldioxastannolane at pH > 9.0. Between pH 5.0 and 9.0, no evidence for any interaction between the diethyltin moiety and the nucleotides was found.
