67154-89-6

Basic information

• Product Name: Silanamine, 1,1,1-trimethyl-N-(2-phenylethenyl)-N-(trimethylsilyl)-, (E)-
• CAS NO: 67154-89-6
• Molecular Formula: C14H25NSi2
• Molecular Weight: 263.53
• Mol File: 67154-89-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Silanamine, 1,1,1-trimethyl-N-(2-phenylethenyl)-N-(trimethylsilyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Silanamine, 1,1,1-trimethyl-N-(2-phenylethenyl)-N-(trimethylsilyl)-, (E)-(67154-89-6)
• EPA Substance Registry System: Silanamine, 1,1,1-trimethyl-N-(2-phenylethenyl)-N-(trimethylsilyl)-, (E)-(67154-89-6)

Safety Data

• Hazardous Substances Data: 67154-89-6(Hazardous Substances Data)

Upstream product

• 4648-54-8 trimethylsilylazide 
• 19372-00-0 1-(trimethylsilyl)-2-phenylethene 
• 122-78-1 phenylacetaldehyde 
• 55147-78-9 bis(bis(trimethylsilyl)amido)tin(II) 
• 75-77-4 chloro-trimethyl-silane 
• 4335-60-8 (E)-cinnamylamine 
• 1450-14-2 1,1,1,2,2,2-hexamethyldisilane 
• 140-29-4 phenylacetonitrile 
• 27607-77-8 trimethylsilyl trifluoromethanesulfonate 

Downstream Products

• 1192591-50-6 C₉H₁₁BN₂O₂ 
• 88765-86-0 1-amino-2-phenylethane-1-boronic acid 
• 1192591-51-7 C₁₀H₁₃BN₂O₂ 

Relevant articles and documents

Synthesis and NMR properties of derivatives of 5,6-dihydroborauracil and 5,6-dihydroborathymine

Novel boron compounds, a series of 4-hydroxy-5,6-dihydroborauracil and 4-hydroxy-5,6-dihydroborathymine derivatives containing various substituents at 3-, 5- and 6-positions, is presented. The spectroscopic properties, along with analyses of NMR-controlled boron compound-alcohol and boron compound-amine interactions, proves the existence of sp3-hybridized, stable B,B-bis-methoxy-5,6-dihydroborauracils and pyridine-/n-butylamine-5,6-dihydroborauracils ate-complexes in solution.

Chemically Labile Stannylene-Nitrogen Bonds. The Chemoselective and Stereoselective Synthesis of N,N-Bis(trimethylsilyl)enamines and N,N-Dialkylenamines

The chemoselective reaction of Sn2 with primary aldehydes leads to the stereoselective synthesis of trans-N,N-bis(trimethylsilyl)enamines.More reactive Sn(NR2)2 (R = Et, iPr, or piperidine) can be generated in situ and then treated with aldehydes or ketones to give trans enamines.