Isopropoxy(triethyl) silane

Base Information

• Chemical Name: Isopropoxy(triethyl) silane
• CAS No.: 1571-45-5
• Molecular Formula: C9H22 O Si
• Molecular Weight: 174.359
• NSC Number: 96836
• DSSTox Substance ID: DTXSID40294502
• Nikkaji Number: J1.202.739G
• Wikidata: Q82033847
• Mol file: 1571-45-5.mol

Synonyms:Isopropoxy(triethyl) silane;1571-45-5;Silane, triethyl(1-methylethoxy)-;triethyl-isopropoxy-silane;triethyl(propan-2-yloxy)silane;NSC96836;SCHEMBL247749;Isopropyl triethylsilyl ether #;DTXSID40294502;UCUKUIPXDKEYLX-UHFFFAOYSA-N;NSC-96836

Chemical Property of Isopropoxy(triethyl) silane

Chemical Property:

• Vapor Pressure: 2.31mmHg at 25°C
• Boiling Point: 166.8°Cat760mmHg
• Flash Point: 43.4°C
• Density: 0.794g/cm³
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 174.143991855
• Heavy Atom Count: 11
• Complexity: 89.5

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[Si](CC)(CC)OC(C)C

Technology Process of Isopropoxy(triethyl) silane

There total 2 articles about Isopropoxy(triethyl) silane 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:

triethyl(propoxy)silane (17841-44-0) + isopropyl alcohol (67-63-0,8013-70-5) → propan-1-ol (71-23-8) + isopropoxytriethylsilane (1571-45-5)

Guidance literature:

With iodine; at 20 ℃; Equilibrium constant; var. temperature;

DOI:10.1246/bcsj.55.2973

Reference yield:

triethylsilane (617-86-7) + acetone (67-64-1) → isopropoxytriethylsilane (1571-45-5) + hexaethyl disiloxane (994-49-0)

Guidance literature:

With ^{2+; +}; hydrogen; at 20 ℃; for 0.25h; rate of hydrogenation; other ketones and alkenes; isomerisation;

DOI:10.1021/ja00117a033

Reference yield:

isopropoxytriethylsilane (1571-45-5) + acetic acid (64-19-7,77671-22-8) → triethylsilyl acetate (5290-29-9) + isopropyl alcohol (67-63-0,8013-70-5)

Guidance literature:

With tris(pentafluorophenyl)borate; In chloroform-d1; at 20 ℃; for 1h;

DOI:10.1002/ejoc.202100982

upstream raw materials:

triethyl(propoxy)silane

isopropyl alcohol

triethylsilane

acetone

Downstream raw materials:

triethyl(propoxy)silane

isopropyl alcohol

triethylsilyl acetate