941-15-1

Basic information

• Product Name: Disilane, 1-chloro-1,1,2,2-tetramethyl-2-phenyl-
• CAS NO: 941-15-1
• Molecular Formula: C10H17ClSi2
• Molecular Weight: 228.869
• Mol File: 941-15-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Disilane, 1-chloro-1,1,2,2-tetramethyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Disilane, 1-chloro-1,1,2,2-tetramethyl-2-phenyl-(941-15-1)
• EPA Substance Registry System: Disilane, 1-chloro-1,1,2,2-tetramethyl-2-phenyl-(941-15-1)

Safety Data

• Hazardous Substances Data: 941-15-1(Hazardous Substances Data)

Upstream product

• 1145-98-8 1,2-diphenyltetramethyldisilane 
• 35107-79-0 1,1,2,2-tetramethyl-2-phenyldisilane 
• 52462-29-0 [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂ 
• 6026-02-4 (N,N-diethylamino)dimethylchlorosilane 
• 3839-31-4 dimethyl(phenyl)silyllithium 
• 4342-61-4 1,2-dichlorotetramethylsilane 
• 591-51-5 phenyllithium 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 144752-33-0 1-(4-Dimethylsilanyl-phenyl)-1,1,2,2-tetramethyl-2-phenyl-disilane 
• 388573-17-9 (CH₃)2Si(C₅H₄Fe(CO)2Si(CH₃)2Si(CH₃)2C₆H₅)2 
• 260995-49-1 C₅H₅FeC₅H₄(Si(CH₃)2)2(C₆H₅) 
• 1379534-76-5 C₂₁H₂₈OSi₂ 
• 69086-14-2 1,1,2,2-Tetramethyl-2-phenyl-1-(3-phenyl-1,3-bis-trimethylsilanyl-propa-1,2-dienyl)-disilane 
• 73022-83-0 {[(Z)-2-(Methoxy-dimethyl-silanyl)-vinyl]-dimethyl-silanyl}-benzene 
• 17881-88-8 methoxydimethylphenylsilane 
• 69053-48-1 1,1,2,2-Tetramethyl-2-phenyl-1-(1-phenyl-3,3-bis-trimethylsilanyl-propa-1,2-dienyl)-disilane 
• 73022-82-9 {[1-(Methoxy-dimethyl-silanyl)-vinyl]-dimethyl-silanyl}-benzene 
• 33716-24-4 1-Bromomethyl-1,1,2,2-tetramethyl-2-phenyl-disilane 
• 81142-39-4 1,1,2,2-tetramethyl-3-phenyl-4-phenyldimethylsilyl-1,2-disilacyclobutene 
• 79628-11-8 1,1-dimethyl-2-phenyl-3-phenyldimethylsilyl-1-silacyclopropene 
• 79628-15-2 dimethyl(phenyl)(phenylethynyl)silane 

Relevant articles and documents

Synthesis and coordination ability of a partially silicon based crown ether

The first hybrid crown ether with two adjacent disilane fragments was synthesized through reaction of O(Si2Me4Cl)2 (3) with O(C2H4OH)2. By means of DFT calculations, the complexation ability of 1,2,4,5-tetrasila[12]crown-4 (7) towards Li+ was determined to be considerably higher compared to [12]crown-4.

London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes

Non-covalent aryl-aryl interactions for the molecular structures of three 1,2-diaryltetramethyldisilanes X5C6-(SiMe2)2-C6Y5 (X ≠ Y; X, Y = H, F, Cl) were studied by single crystal X-ray and

Ruthenium-catalyzed alkoxylation of a hydrodisilane without Si[sbnd]Si bond cleavage

Transition metal-catalyzed synthesis of alkoxydisilanes via dehydrogenative coupling of a hydrodisilane with alcohols is reported. During the reaction, the Si[sbnd]Si bond is preserved effectively when [RuCl2(p-cymene)]2is used as a catalyst. Various alcohols can be used in this alkoxylation.