(2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane

Base Information

• Chemical Name: (2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane
• CAS No.: 10217-34-2
• Molecular Formula: C14H28O4Si
• Molecular Weight: 288.459
• Hs Code.: 2932999099
• European Community (EC) Number: 425-050-4,600-284-1
• DSSTox Substance ID: DTXSID7044762
• Nikkaji Number: J185.747I
• ChEMBL ID: CHEMBL3187959
• Mol file: 10217-34-2.mol

Synonyms:10217-34-2;(2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane;2-(3,4-Epoxycyclohexyl)ethyltriethoxysilane;CCRIS 3045;C14H28O4Si;2-(3,4-epoxycyclohexyl)ethyltriethoxy silane;beta-(3,4-Epoxycyclohexyl)ethyltriethoxysilane;triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane;7-Oxabicyclo[4.1.0]heptane, 3-[2-(triethoxysilyl)ethyl]-;DTXSID7044762;TRIETHOXY-[2-(7-OXABICYCLO[4.1.0]HEPTAN-3-YL)ETHYL]SILANE;7-Oxabicyclo(4.1.0)heptane, 3-(2-(triethoxysilyl)ethyl)-;EC 425-050-4;Silane, triethoxy(2-(7-oxabicyclo(4.1.0)hept-3-yl)ethyl)-;Silane, triethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]-;Triethoxy[2-(7-oxabicyclo[4.1.0]heptan-3-yl)ethyl]silane;SCHEMBL48916;CHEMBL3187959;DTXCID5024762;C14-H28-O4-Si;Triethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane;Tox21_300751;MFCD00069159;NCGC00248158-01;NCGC00254656-01;CAS-10217-34-2;LS-194125;LS-194260;LS-194913;FT-0697185;T3585;2-(3,4-epoxycyclohexyl) ethyltriethoxysilane;2-(3,4-epoxycyclohexyl)-ethyltriethoxysilane;2-(3,4-epoxycyclohexyl)ethyl triethoxysilane;D92722;Y-4036;A896879;[2-(3,4-Epoxycyclohexane-1-yl)ethyl]triethoxysilane;2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, AldrichCPR

Chemical Property of (2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane

Chemical Property:

• Vapor Pressure: 0.000767mmHg at 25°C
• Refractive Index: 1.4455
• Boiling Point: 316.319 °C at 760 mmHg
• Flash Point: 117.725 °C
• PSA: 40.22000
• Density: 1.003 g/cm³
• LogP: 2.99240
• Storage Temp.: 2-8°C
• Water Solubility.: 850mg/L at 20℃
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 9
• Exact Mass: 288.17568590
• Heavy Atom Count: 19
• Complexity: 257

Purity/Quality:

99% ^*data from raw suppliers

2-(3,4-Epoxycyclohexyl)ethyltriethoxysilane ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-28-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCO[Si](CCC1CCC2C(C1)O2)(OCC)OCC

Technology Process of (2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane

There total 3 articles about (2-(7-Oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

1,2-Epoxy-4-vinylcyclohexane (106-86-5) + Triethoxysilane (998-30-1) → (2-(7-oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane (10217-34-2)

Guidance literature:

With platinum-containing olefin organic polymer catalyst; at 25 ℃; for 3h;

Reference yield: 96.0%

→ (2-(7-oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane (10217-34-2)

Guidance literature:

With (^TFAPDI)Co(2-ethylhexanoate)₂; at 20 ℃; for 1h;

Reference yield:

1,2-Epoxy-4-vinylcyclohexane (106-86-5) → (2-(7-oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane (10217-34-2)

Guidance literature:

With dihydrogen hexachloroplatinate; tert-butyl alcohol; at 140 ℃; Behandeln des Reaktionsgemisches mit Triaethoxy-silan;

DOI:10.1021/ja01520a008

upstream raw materials:

1,2-Epoxy-4-vinylcyclohexane

Triethoxysilane

Refernces

• 1、 Kanda, Yasuharu,Kondo, Ryota,Lin, Xianjin,Nagata, Tatsuki,Obora, Yasushi,Shimizu, Ken-ichi,Suzuki, Takeyuki,Tanaka, Tatsuya,Toyao, Takashi. "N,N-Dimethylformamide-protected Fe2O3 Combined with Pt Nanoparticles: Characterization and Catalysis in Alkene Hydrosilylation". . . Retrieved 2021/11/30.
• 2、 Liu, Yang,Deng, Liang. "Mode of activation of cobalt(II) amides for catalytic hydrosilylation of alkenes with tertiary silanes". supporting information. p. 1798 - 1801. Retrieved 2017/02/15.