Isopropoxytrimethylsilane

Base Information

• Chemical Name: Isopropoxytrimethylsilane
• CAS No.: 1825-64-5
• Molecular Formula: C6H16 O Si
• Molecular Weight: 132.278
• Hs Code.: 2931900090
• European Community (EC) Number: 217-372-7
• DSSTox Substance ID: DTXSID00171300
• Nikkaji Number: J132.713E
• Wikidata: Q27145894
• Mol file: 1825-64-5.mol

Synonyms:Isopropoxytrimethylsilane;1825-64-5;Trimethyl(1-methylethoxy)silane;trimethyl(propan-2-yloxy)silane;Silane, trimethyl(1-methylethoxy)-;Silane, isopropoxytrimethyl-;Isopropyl trimethylsilyl ether;Trimethylisopropoxysilane;Isopropyl alcohol, TMS derivative;EINECS 217-372-7;isopropoxy(trimethyl)silane;O-TMS-isopropanol;i-PrOTMS;2-Propoxytrimethylsilane;Me2CH(OTMS);O-trimethylsilylisopropanol;trimethyl-2-propoxy silane;SCHEMBL276184;Isopropoxytrimethylsilane, 98%;CHEBI:76336;DTXSID00171300;MFCD00134520;AKOS025404555;AS-77665;FT-0633865;I1133;D95456;J-011682;J-802044;Q27145894

Chemical Property of Isopropoxytrimethylsilane

Chemical Property:

• Vapor Pressure: 52.8mmHg at 25°C
• Refractive Index: n20/D 1.378(lit.)
• Boiling Point: 95 °C at 760 mmHg
• Flash Point: 12 °F
• PSA: 9.23000
• Density: 0.745 g/mL at 25 °C(lit.)
• LogP: 2.24630
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 132.097041664
• Heavy Atom Count: 8
• Complexity: 63.4

Purity/Quality:

98% ^*data from raw suppliers

Isopropoxytrimethylsilane 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F
• Hazard Codes: F
• Statements: 11
• Safety Statements: 16-36/37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(C)O[Si](C)(C)C

Technology Process of Isopropoxytrimethylsilane

There total 48 articles about Isopropoxytrimethylsilane 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: 94.0%

3-(trimethylsilyl)-2-oxazolidinone (43112-38-5) + isopropyl alcohol (67-63-0,8013-70-5) → isopropoxytrimethylsilane (1825-64-5)

Guidance literature:

at 20 ℃; for 0.0166667h;

Reference yield: 90.4%

trimethyl-(1H,1H,3H-tetrafluoropropoxy)silane (56002-69-8) + isopropyl alcohol (67-63-0,8013-70-5) → isopropoxytrimethylsilane (1825-64-5)

Guidance literature:

at 20 ℃; for 1h;

Reference yield: 85.7%

chloro-trimethyl-silane (75-77-4) + isopropyl alcohol (67-63-0,8013-70-5) → isopropoxytrimethylsilane (1825-64-5)

Guidance literature:

With urea; at 20 ℃; for 4h;

upstream raw materials:

chloro-trimethyl-silane

isopropyl alcohol

9-(trimethylsilyl)fluorene

sodium isopropylate

Downstream raw materials:

Trimethylmethoxysilane

isopropyl triflate

2-Isopropoxycyclohex-2-en-1-on

hexamethyldisilathiane

Refernces

• 1、 Vertes et al.. "". . p. 149. Retrieved 1975.
• 2、 Beaumont et al.. "". . p. 671. Retrieved 1966.
• 3、 Chauvier, Clément,Godou, Timothé,Cantat, Thibault. "Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates". supporting information. p. 11697 - 11700. Retrieved 2017/11/03.
• 4、 Dey, Rupa Rani,Dhar, Siddhartha Sankar. "Synthesis and characterization of 2-carboxyethyltriphenyl phosphonium tribromide and its application as catalyst in silylation of alcohols and thiols under solvent-free condition". supporting information. p. 2355 - 2363. Retrieved 2014/07/22.