85952-93-8

Basic information

• Product Name: 2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane-1-propanamine, N-pheny l-
• Synonyms: 2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane-1-propanamine, N-pheny l-
• CAS NO: 85952-93-8
• Molecular Formula: C₁₅H₂₄N₂O₃Si
• Molecular Weight: 308.4482
• Mol File: 85952-93-8.mol

Chemical Properties

• Melting Point: 142.1 °C
• Boiling Point: 438.2°Cat760mmHg
• Flash Point: 218.8°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 7.06E-08mmHg at 25°C
• Refractive Index: 1.552
• PKA: 6.92±0.20(Predicted)
• CAS DataBase Reference: 2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane-1-propanamine, N-pheny l-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane-1-propanamine, N-pheny l-(85952-93-8)
• EPA Substance Registry System: 2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane-1-propanamine, N-pheny l-(85952-93-8)

Safety Data

• Hazardous Substances Data: 85952-93-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H24N2O3Si/c1-2-5-15(6-3-1)16-7-4-14-21-18-11-8-17(9-12-19-21)10-13-20-21/h1-3,5-6,16H,4,7-14H2

Upstream product

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Relevant articles and documents

Synthesis of 1-arylaminopropyl silatranes

Ten 1-substituted arylaminopropyl silatranes (I - X) were synthesized by the reaction of aromatic amines with chloropropyl silatrane and aryl chloride with aminopropyl silatrane respectively. Their structures were identified by elemental analysis, IR, su

Synthesis and structural characterization of first adenine containing organosilicon nucleobase for the recognition of Cu2+ ion

This work reports the synthesis and structural characterization of a new adenine based organosilicon nucleobase using an efficient and biocompatible Click approach. Synthetic procedure included the preparation of a new N-acetylinic linked propyl silatrane 3 whose structure was confirmed through Single crystal X-ray crystallography. The designed silatrane L is found to be highly selective and sensitive for detection of Cu2+ with a color change from colourless to yellowish orange. The stoichiometry ratio of L + Cu2+ was obtained 1:1 by Job's Plot. The binding of copper ions to the chemosensor was studied over wide pH range and the results demonstrated that the sensor worked well in the physiological range 6–9. Furthermore, the sensing of Cu2+ was found to be reversible upon addition of EDTA. These results widen the scope of adenine based derivatives in the field of colorimetric probes. The newly synthesized silatrane 3 and the receptor L were successfully characterized by various spectroscopic techniques [IR, NMR (1H, 13C) and Mass] and elemental analysis.