444122-23-0

Basic information

• Product Name: (R)-1,2,2,2-tetramethyl-1-phenyl-1-(piperidinomethyl)disilane
• Synonyms: (R)-1,2,2,2-tetramethyl-1-phenyl-1-(piperidinomethyl)disilane
• CAS NO: 444122-23-0
• Molecular Weight: 291.584
• Mol File: 444122-23-0.mol

Chemical Properties

• CAS DataBase Reference: (R)-1,2,2,2-tetramethyl-1-phenyl-1-(piperidinomethyl)disilane(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1,2,2,2-tetramethyl-1-phenyl-1-(piperidinomethyl)disilane(444122-23-0)
• EPA Substance Registry System: (R)-1,2,2,2-tetramethyl-1-phenyl-1-(piperidinomethyl)disilane(444122-23-0)

Safety Data

• Hazardous Substances Data: 444122-23-0(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 444122-20-7 (R)-1,2-dimethyl-1,2,2-triphenyl-1-(piperidinylmethyl)disilane 

Downstream Products

• 92-52-4 biphenyl 
• 1361114-22-8 C₁₆H₂₉NSi₂ 

Relevant articles and documents

Synthesis of a highly enantiomerically enriched silyllithium compound

The highly enantiomerically enriched silyllithium compound lithiomethylphenyl(1-piperidinylmethyl)silane (4) reacts stereospecifically with chlorosilanes, but over a period of several hours slow racemization in solution at room temperature occurs, which c

A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium

(Chemical Equation Presented) On the path to chiral polysilanes, the synthesis and first structural characterization of the enantiomerically pure tetrasilane (R)-3 was achieved. A new synthetic strategy was used, by which the cleavage of a silicon-phenyl