193417-26-4 Usage
General Description
N-[3-(triethoxysilyl)propyl]-2-carbomethoxyaziridine is a chemical compound that belongs to the group of organosilanes. It is commonly used as a crosslinking agent in the production of silicone rubber, sealants, and adhesives. The triethoxysilyl functional group in the molecule allows it to bond strongly with silica and other inorganic materials, making it particularly useful in applications that require adhesion to various substrates. Additionally, its aziridine moiety provides it with reactivity towards a range of nucleophiles, enabling it to participate in various synthetic processes. Overall, this compound plays a crucial role in the formulation of materials with enhanced mechanical properties and improved durability.
Check Digit Verification of cas no
The CAS Registry Mumber 193417-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,1 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 193417-26:
(8*1)+(7*9)+(6*3)+(5*4)+(4*1)+(3*7)+(2*2)+(1*6)=144
144 % 10 = 4
So 193417-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H27NO5Si/c1-5-17-20(18-6-2,19-7-3)10-8-9-14-11-12(14)13(15)16-4/h12H,5-11H2,1-4H3
193417-26-4Relevant articles and documents
Molecular recognition by a silica-bound fullerene derivative
Bianco, Alberto,Gasparrini, Francesco,Maggini, Michele,Misiti, Domenico,Polese, Alessandra,Prato, Maurizio,Scorrano, Gianfranco,Toniolo, Claudio,Villani, Claudio
, p. 7550 - 7554 (1997)
Thermal ring opening of N-[3-(triethoxysilyl)propyl]-2-carbomethoxyaziridine in the presence of C60 produces a fulleropyrrolidine derivative which is then attached covalently to HPLC silica gel. The new chromatographic material is used to investigate binding affinities of potential hosts for the immobilized C60 Exceptionally high size selectivities have been obtained for cyclic oligomeric compounds like calixarenes and cyclodextrins in organic and water-rich media, respectively. A number of rationally designed, helical-shaped peptides bind selectively to the grafted fullerene. The most tightly bound peptide carries two ferrocene moieties at the periphery of a hydrophobic binding cavity complementary in size to C60.
