2060-89-1

Basic information

• Product Name: 1,3-BIS(TRIMETHYLSILYL)BENZENE
• Synonyms: Trimethyl[2-(trimethylsilyl)phenyl]silane;1,3-BIS(TRIMETHYLSILYL)BENZENE
• CAS NO: 2060-89-1
• Molecular Formula: C₁₂H₂₂Si₂
• Molecular Weight: 222.47
• Mol File: 2060-89-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 120℃/25mm
• Flash Point: >60°(140°F)
• Appearance: /Liquid
• Density: 0.85 g/cm³
• Refractive Index: 1.482
• CAS DataBase Reference: 1,3-BIS(TRIMETHYLSILYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-BIS(TRIMETHYLSILYL)BENZENE(2060-89-1)
• EPA Substance Registry System: 1,3-BIS(TRIMETHYLSILYL)BENZENE(2060-89-1)

Safety Data

• Hazardous Substances Data: 2060-89-1(Hazardous Substances Data)

Usage

General Description

1,3-Bis(trimethylsilyl)benzene is a chemical compound with the molecular formula C14H26Si2. It is a colorless liquid and is commonly used as a building block in organic synthesis. Due to its highly reactive nature, it is often used as a precursor in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is also used as a protecting group for alcohols and phenols in organic chemistry. It is important to handle this compound with caution, as it is flammable and can cause skin and eye irritation upon contact.

InChI:InChI=1S/C12H22Si2/c1-13(2,3)11-9-7-8-10-12(11)14(4,5)6/h7-10H,1-6H3

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 71-43-2 benzene 
• 18090-43-2 3,6-bis(trimethylsilyl)cyclohexane-1,4-diene 
• 541-73-1 1,3-Dichlorobenzene 
• 4405-42-9 m-chlorophenyltrimethylsilane 
• 15842-76-9 (2-chloro-phenyl)-trimethyl-silane 

Downstream Products

• 55562-93-1 3-Trimethylsilyl-benzolsulfonsaeure-trimethylsilylester 
• 55499-82-6 C₁₂H₂₂O₆S₂Si₂ 
• 626-00-6 1,3-Diiodobenzene 
• 63520-49-0 1-Iod-3-(trimethylsilyl)benzol 
• 73178-04-8 Toluene-4-sulfonatephenyl-(3-trimethylsilanyl-phenyl)-iodonium; 
• 15290-24-1 3-nitro-1-(trimethylsilyl)benzene 
• 78627-92-6 1-nitro-2,4-bis(trimethylsilyl)benzene 
• 125973-47-9 1,3-dinitro-5-trimethylsilylbenzene 
• 17983-62-9 1-[3-(trimethylsilyl)phenyl]ethanone 
• 18257-89-1 1-allyl-3-bromo-benzene 
• 107134-82-7 1,3-bis(dibromoboryl)benzene 
• 107134-71-4 [3-(dichloroboryl)phenyl]trimethylsilane 
• 172220-16-5 ((CH₃)5C₅)Rh(P(CH₃)3)(H)(C₆H₃(Si(CH₃)3)2) 
• 135129-91-8 3,5-bis(trimethylsilyl)trifluoroacetophenone 

Relevant articles and documents

Theory and practice: Bulk synthesis of C3B and its H2- and Li-storage capacity

Previous theoretical studies of C3B have suggested that boron-doped graphite is a promising H2- and Li-storage material, with large maximum capacities. These characteristics could lead to exciting applications as a lightweight H

Retinobenzoic Acids. 5. Retinoidal Activities of Compounds Having a Trimethylsilyl or Trimethylgermyl Group(s) in Human Promyelocytic Leukemia Cells HL-60

The retinoidal activities of trimethylsilyl or trimethylgermyl-containing retinobenzoic acids are discussed on the basis of differentiation-inducing activity on human promyelocytic leukemia cells HL-60.Compounds with a trimethylsilyl or trimethylgermyl gr

ELECTRON SPIN RESONANCE AND CHEMICAL STUDIES ON THE 6-(TRIMETHYLSILYL)CYCLOHEXADIENYL AND RELATED RADICALS.

Various 3,6-disubstituted cyclohexadienyl radicals were generated and investigated by ESR at low temperature. Analysis of the ESR parameters indicated that the significant out-of-plane deformation of the carbon framework of 6-Me//3Si- and 6-Me//3Ge-substituted cyclohexadienyl radicals occurred to gain stabilization due to the effective hyperconjugation between the substituted methylene pseudo- pi orbital and the pi SOMO, while the 6-unsubstituted and 6-t-Bu cyclohexadienyl radicals were essentially planar. Investigation of the fate of the 3,6-bis(trimethylsilyl)cyclohexadienyl radical showed strong evidence for the temperature-dependent reversibility of the silyl radical addition to aromatics. The spontaneous elimination of the trimethylsilyl radical was proved by spin-trapping experiments.