2587-46-4 Usage
Uses
Used in Silicone Polymer Production:
1,2,3,4,5,6-Hexamethylcyclo trisilazane is used as a cross-linking agent for enhancing the properties of silicone polymers, contributing to their overall performance and durability.
Used in Organosilicon Compound Synthesis:
In the chemical industry, 1,2,3,4,5,6-Hexamethylcyclo trisilazane serves as a key intermediate in the synthesis of various organosilicon compounds, which have diverse applications in different fields.
Used in Semiconductor Material Manufacturing:
1,2,3,4,5,6-HEXAMETHYLCYCLOTRISILAZANE is utilized in the production of semiconductor materials due to its thermal stability and resistance to oxidation, which are critical for the performance of semiconductor devices.
Used in Coating Production:
1,2,3,4,5,6-Hexamethylcyclo trisilazane is used as a component in the manufacturing of coatings that require high heat resistance and oxidation resistance, making it suitable for applications where such properties are essential.
Used in Electronics Industry:
1,2,3,4,5,6-Hexamethylcyclo trisilazane is employed as a high-performance insulating material in the electronics industry, leveraging its unique properties to ensure the reliable functioning of electronic components and devices.
Used in Aerospace Industry:
In the aerospace sector, 1,2,3,4,5,6-HEXAMETHYLCYCLOTRISILAZANE is used for its insulating properties, contributing to the performance and safety of aerospace materials and components, particularly in high-stress environments where thermal and oxidative stability are paramount.
Check Digit Verification of cas no
The CAS Registry Mumber 2587-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2587-46:
(6*2)+(5*5)+(4*8)+(3*7)+(2*4)+(1*6)=104
104 % 10 = 4
So 2587-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H21N3Si3/c1-7-10(4)8(2)12(6)9(3)11(7)5/h10-12H,1-6H3
2587-46-4Relevant academic research and scientific papers
Bis(chloromethylsilyl)amine and bis(chloromethylsilyl)methylamine; preparation, reactivity and spectroscopic studies of their stereoisomers and conformers
Fleischer, Holger,McKean, Donald C.,Pulham, Colin R.,Buehl, Michael
, p. 585 - 592 (2007/10/03)
The compounds NH(SiHMeCl)2 I and NMe(SiHMeCl)2 2 have been prepared by treating SiHMeCl2 with CaCl2·8NH3 and NH2Me respectively. Each was characterised by elemental analysis, mass spectrometry, NMR and IR spectroscopy. Dipole moments were also measured. The NMR spectra indicate that both compounds form 1:1 mixtures of the rac and meso diastereomers, their abundances corresponding to a statistically controlled synthetic pathway. The NMR and mass spectra also show that 1,5-dichloro-1,2,3,4,5-pentamethyltrisilazane, SiHMe[NMe(SiHMeCl)]2 3, which is formed as a side product in the synthesis of 2, also consists of two diastereomers. Variable-temperature 1H NMR spectra of NH(SiHMeCl)2 indicate participation of H(N) in hydrogen bonding. The compound is decomposed by heat and reacts with pyridine to form NH4Cl, SiHMeCl2 and polysilazanes, whereas NMe(SiHMeCl)2 shows only slight decomposition up to 80°C and does not react with pyridine. Infrared spectra in the v(SiH) region are interpreted in terms of the results of ab initio calculations of frequency, intensity and conformer abundance. The two bands near 2200 cm-1 in the spectrum of 2 have their origin in two effects: different orientations of the Si-H bonds relative to the Si-N-Si plane in several conformers and an unprecedented strong dipole-dipole coupling between the two Si-H bond stretching motions in situations where the bonds are roughly parallel. The absence of such an observed splitting for 1 is likely to be due in part to signal averaging during a free internal rotation. Significant couplings are also calculated to occur between Si-Cl bond-stretching motions, whose source must be different from that for the Si-H bond stretches.
