76710-52-6

Basic information

• Product Name: Methanamine, N,N-di(2-trimethylsilyloxyethyl)-
• Synonyms: Methanamine, N,N-di(2-trimethylsilyloxyethyl)-
• CAS NO: 76710-52-6
• Molecular Formula: C₁₁H₂₉NO₂Si₂
• Molecular Weight: 0
• Mol File: 76710-52-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 231.9°C at 760 mmHg
• Flash Point: 94°C
• Appearance: /
• Density: 0.873g/cm³
• Vapor Pressure: 0.0609mmHg at 25°C
• Refractive Index: 1.428
• CAS DataBase Reference: Methanamine, N,N-di(2-trimethylsilyloxyethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanamine, N,N-di(2-trimethylsilyloxyethyl)-(76710-52-6)
• EPA Substance Registry System: Methanamine, N,N-di(2-trimethylsilyloxyethyl)-(76710-52-6)

Safety Data

• Hazardous Substances Data: 76710-52-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H29NO2Si2/c1-12(8-10-13-15(2,3)4)9-11-14-16(5,6)7/h8-11H2,1-7H3

Upstream product

• 105-59-9 N-Methyldiethanolamine 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 66586-09-2 1,1-diphenyl-5-methylquasisilatrane 
• 1003612-57-4 1-phenyl-1-fluoro-5-methylquasisilatrane 
• 358-21-4 perfluorodiethyl ether 
• 382-27-4 Perfluoro-N,N-dimethylaminoacetyl fluoride 
• 382-28-5 2,2,3,3,5,5,6,6-Octafluoro-4-trifluoromethyl-morpholine 
• 250688-32-5 Perfluoro-[N,N-bis(fluorocarbonylmethyl)methylamine] 
• 66583-27-5 2,2-diphenyl-6-methyl-1,3-dioxa-6-aza-2-silacyclooctane 

Relevant articles and documents

Intramolecular base-stabilised adducts of main group halides

The coordination chemistry of alkoxo and amido ligands bearing pendant nitrogen or sulfur donors has been developed to include examples of main group complexes. The structural implications of amido ligand coordination augmented by a tethered pyridyl base have been investigated for group 13 and 14 derivatives {[6-(Me3SiN)-2-Me-C5H3N]SnCl3 and [6-(Me3SiN)-2-Me-C5H3N]BBr2}. Furthermore, the scope, kinetics and mechanism of the synthesis of alkoxo and amido derivatives from trimethylsilyl substituted precursors have been investigated in depth. The methodology is found to be applicable to a range of ligand frameworks of varying flexibility, stabilised by one or two "tether" arms.