tert-Butyldimethylsilyl (R)-(-)-glycidyl ether

Base Information

• Chemical Name: tert-Butyldimethylsilyl (R)-(-)-glycidyl ether
• CAS No.: 124150-87-4
• Molecular Formula: C9H20 O2 Si
• Molecular Weight: 188.342
• Hs Code.: 2931900090
• European Community (EC) Number: 602-982-1
• DSSTox Substance ID: DTXSID70451681
• Nikkaji Number: J881.662J
• Wikidata: Q82271821
• Mol file: 124150-87-4.mol

Synonyms:124150-87-4;tert-Butyldimethylsilyl (R)-(-)-glycidyl ether;(R)-tert-butyldimethyl(oxiran-2-ylmethoxy)silane;tert-Butyldimethylsilyl (R)-Glycidyl Ether;tert-butyl-dimethyl-[[(2R)-oxiran-2-yl]methoxy]silane;SCHEMBL632976;DTXSID70451681;YANSSVVGZPNSKD-MRVPVSSYSA-N;ZEA15087;AC8380;MFCD01862148;AKOS025294219;CS-W016779;AS-72043;(r)-tert-butyl-dimethyl-oxiranylmethoxy-silane;tert-Butyldimethylsilyl(R)-(-)-glycidylether;2beta-[(tert-Butyldimethylsiloxy)methyl]oxirane;TERT-BUTYLDIMETHYLSILYL(R)-(-)-GLYCIDY&;A890590;TERT-BUTYLDIMETHYLSILYL (R)-(-)-GLYCIDY&;J-005046;tert-butyl(dimethyl)[(2R)-oxiran-2-ylmethoxy]silane;tert-butyldimethyl{[(2R)-oxiran-2-yl]methoxy}silane;tert-Butyldimethylsilyl (R)-(-)-glycidyl ether, 98%;Oxirane, 2-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-, (2R)-

Chemical Property of tert-Butyldimethylsilyl (R)-(-)-glycidyl ether

Chemical Property:

• Vapor Pressure: 0.298mmHg at 25°C
• Refractive Index: n20/D 1.4310
• Boiling Point: 195-199 °C/760 mmHg
• Flash Point: 74 °C
• PSA: 21.76000
• Density: 0.870 g/mL at 25 °C
• LogP: 2.40700
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 188.123256411
• Heavy Atom Count: 12
• Complexity: 160

Purity/Quality:

98% or more ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)[Si](C)(C)OCC1CO1
• Isomeric SMILES: CC(C)(C)[Si](C)(C)OC[C@H]1CO1

Technology Process of tert-Butyldimethylsilyl (R)-(-)-glycidyl ether

There total 22 articles about tert-Butyldimethylsilyl (R)-(-)-glycidyl ether 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: 100.0%

tert-butyldimethylsilyl chloride (18162-48-6) + (R)-oxiranemethanol (57044-25-4) → tert-butyldimethylsilyl (S)-glycidyl ether (78906-15-7,114413-26-2,124150-87-4,123237-62-7)

Guidance literature:

With 1H-imidazole; triethylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1002/chem.200802681

Reference yield: 95.0%

oxiranyl-methanol (556-52-5) + tert-butyldimethylsilyl chloride (18162-48-6) → tert-butyldimethylsilyl glycidyl ether (114413-26-2,123237-62-7,124150-87-4,78906-15-7)

Guidance literature:

With 1H-imidazole; In tetrahydrofuran; at 20 ℃; Inert atmosphere;

DOI:10.1021/ol401787n

Reference yield: 73.0%

Allyloxy-tert-butyl-dimethyl-silane (85807-85-8) → tert-butyldimethylsilyl glycidyl ether (114413-26-2,123237-62-7,124150-87-4,78906-15-7)

Guidance literature:

With sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; Ambient temperature;

DOI:10.1016/S0040-4020(01)86217-7

upstream raw materials:

Allyloxy-tert-butyl-dimethyl-silane

oxiranyl-methanol

tert-butyldimethylsilyl chloride

1H-imidazole

Downstream raw materials:

(2S,4R)-2-Benzyl-5-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-pentanoic acid ((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide

tert-butyldimethylsilyl (S)-glycidyl ether

(R)-3-((tert-butyldimethylsilyl)oxy)propane-1,2-diol

1-(tert-butyldimethylsiloxy)-2-propanone

Refernces

• 1、 Lu, Benjamin L.,Williams, Geoffrey M.,Verdon, Daniel J.,Dunbar, P. Rod,Brimble, Margaret A.. "Synthesis and Evaluation of Novel TLR2 Agonists as Potential Adjuvants for Cancer Vaccines". supporting information. p. 2282 - 2291. Retrieved 2019/10/02.
• 2、 Alford, Morgan A.,Tian, Zhenlin,Menard, Frederic,Klegeris, Andis. "Characterization of novel kainic acid analogs as inhibitors of select microglial functions". . p. 25 - 35. Retrieved 2019/03/04.