83569-22-6

Basic information

• Product Name: (C₆H₅)3SnCu
• Synonyms: (C₆H₅)3SnCu
• CAS NO: 83569-22-6
• Molecular Weight: 413.573
• Mol File: 83569-22-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (C₆H₅)3SnCu(CAS DataBase Reference)
• NIST Chemistry Reference: (C₆H₅)3SnCu(83569-22-6)
• EPA Substance Registry System: (C₆H₅)3SnCu(83569-22-6)

Safety Data

• Hazardous Substances Data: 83569-22-6(Hazardous Substances Data)

Upstream product

• 4167-90-2 triphenylstannyllithium 
• 7787-70-4 copper(I) bromide 

Downstream Products

• 4104-90-9 allenyltriphenylstannane 
• 85366-29-6 2-(triphenylstannyl)-4-methyl-2,3-pentadiene 
• 85366-25-2 1-(triphenylstannyl)-3,3-tetramethylenepropadiene 
• 85366-23-0 1-(triphenylstannyl)-3-methyl-1,2-butadiene 
• 85366-27-4 1-(triphenylstannyl)-3,3-pentamethylenepropadiene 
• 85366-34-3 (C₆H₅)3Sn(CH₃)CCCHC₃H₇ 
• 85366-34-3 CH₃C₂CHC₃H₇Sn(C₆H₅)3 
• 85366-22-9 1-(triphenylstannyl)-3-phenyl-1,2-propadiene 

Relevant articles and documents

REGIO- AND STEREO-CHEMICAL FEATURES OF THE STANNYLCOPPER(I)-INDUCED SUBSTITUTION IN PROPARGYLIC SUBSTRATES

Stannylcopper(I) species, R3SnCu and 2CuLi, preferentially convert propargylic substrates, R1CCCR2R3X (X=Br, MeCO2, MeS(O)O or MeSO3) into allenes R3Sn(R1)C=C=CR2R3.Only when the group R1 causes much greater steric hindrance than with R2 and R3 is the acetylenic product R1CCCR2R3SnR3 formed.The stereochemical course of the allene formation has been studied in both the steroid and non-steroid series, and found to be mainly or exclusively anti.