96481-36-6

Basic information

• Product Name: Germane, difluorobis(2,4,6-trimethylphenyl)-
• CAS NO: 96481-36-6
• Molecular Formula: C18H22F2Ge
• Molecular Weight: 348.959
• Mol File: 96481-36-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Germane, difluorobis(2,4,6-trimethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Germane, difluorobis(2,4,6-trimethylphenyl)-(96481-36-6)
• EPA Substance Registry System: Germane, difluorobis(2,4,6-trimethylphenyl)-(96481-36-6)

Safety Data

• Hazardous Substances Data: 96481-36-6(Hazardous Substances Data)

Upstream product

• 14104-20-2 silver tetrafluoroborate 
• 96481-42-4 dichlorodimesitylgermane 
• 143367-75-3 N-dimesitylfluorogermyl-N-tri-t-butyl-2,4,6-phenylamine 
• 136948-87-3 mesityltrifluorogermane 
• 106092-68-6 dimesityldimethoxygermane 

Downstream Products

• 96481-37-7 (dimesityl)fluorogermyl(2,4,6-butylphenyl)phosphine 
• 177902-38-4 ((CH₃)3C₆H₂)2Ge(F)(C(Br)PC₆H₂(C(CH₃)3)3) 
• 1220911-71-6 bis(2,4,6-trimethylphenyl)-2,7-di-tert-butylfluorenylidenegermane 
• 956146-20-6 ((CH₃)3C₆H₂)2Ge(OCH₃)CHCl₂ 
• 204134-66-7 3,7-diphenyl-2,2,6,6-tetrakis(2,4,6-trimethylphenyl)-2,6-digerma-1,5-diazacyclooctatetra-3,4,7,8-ene 
• 204134-68-9 (fluorodimesitylgermyl)methylphenylacetonitrile 
• 1220911-72-7 bis(2,4,6-trimethylphenyl)-2,7-di-tert-butylfluorenyl(fluoro)germane 
• 956146-17-1 dimesitylfluoro(trichloro)germane 
• 169053-41-2 N-dimesitylfluoroogermyl N-2,4,6-trifluoroaniline 
• 177902-42-0 ((CH₃)3C₆H₂)2Ge(F)C(H)PC₆H₂(C(CH₃)3)3 
• 204134-69-0 (fluorodimesitylgermyl)phenylacetonitrile 
• 146699-06-1 ((CH₃)3C₆H₂)2Ge(F)NHC₆H₄CON(CH₃)2 
• 143445-88-9 dimesitylvinylfluorogermane 
• 143367-74-2 N-dimesitylfluorogermyl-N-mesitylamine 

Relevant articles and documents

Addition of Organometallic Reagents to a Stable Silene and Germene

A variety of alkyllithium (R = Me, Bu, t-Bu) reagents and potassium tert-butoxide were added to the highly reactive silene Mes2Si=CHCH2t-Bu (1) and the germene Mes2Ge=CHCH2t-Bu (4) in diethyl ether. 1,2-Addition products were obtained regioselectively and in good yield after treatment with a weak acid with no evidence for any rearrangement products and no polymerization observed. The reactivity of the silene 1 and germene 4 toward organometallic reagents is compared to previous studies of analogous silenes and germenes. (Chemical Equation Presented).