226890
2-(Trimethylsilyl)ethanol
96%
Synonym(s):
(2-Hydroxyethyl)trimethylsilane
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
(CH3)3SiCH2CH2OH
CAS Number:
Molecular Weight:
118.25
Beilstein/REAXYS Number:
1732034
EC Number:
MDL number:
UNSPSC Code:
12352000
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
96%
form
liquid
refractive index
n20/D 1.423 (lit.)
bp
71-73 °C/35 mmHg (lit.)
density
0.825 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(C)CCO
InChI
1S/C5H14OSi/c1-7(2,3)5-4-6/h6H,4-5H2,1-3H3
InChI key
ZNGINKJHQQQORD-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Protecting reagent for carboxyl and phosphate groups.
Used to synthesize Teoc-protected amines via alcoholysis of the corresponding isocyanates.
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Tetrahedron Letters, 33, 7685-7685 (1992)
Tetrahedron Letters, 35, 757-757 (1994)
Seth L Crawley et al.
Organic letters, 8(18), 3995-3998 (2006-08-25)
A new protocol for generating aza-ortho-xylylenes via acid-catalyzed or fluoride-promoted ring opening of 2-(2-acylaminophenyl)aziridines is described. This methodology has been exploited in the rapid construction of a hexacyclic substructure of communesin B.
A Aberman et al.
Biochimica et biophysica acta, 791(2), 278-280 (1984-12-07)
Several trimethylsilyl derivatives were found to be ligands of acetylcholinesterase (acetylcholine acetylhydrolase, EC 3.1.1.7): trimethylsilylethyl acetate (III) and trimethylsilylmethyl acetate (V) are substrates of the enzyme, whereas trimethylsilylethanol (VIII) is a competitive inhibitor. The silicon compounds have kinetic parameters similar
Journal of the Chemical Society. Perkin Transactions 1, 2639-2639 (1993)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service