Skip to Content
MilliporeSigma
All Photos(1)

Documents

519324

Sigma-Aldrich

1-(tert-Butyldimethylsilyloxy)-1-methoxyethene

97%

Synonym(s):

(1,1-Dimethylethyl)[(1-methoxyethenyl)oxy]dimethylsilane, (tert-Butyl)[(1-methoxyethenyl)oxy]dimethylsilane, 1-Methoxy-1-(tert-butyldimethylsiloxy)ethylene, 1-Methoxy-1-[(tert-butyldimethylsilyl)oxy]ethene, 1-Methoxy-1-[(tert-butyldimethylsilyl)oxy]ethylene, Ketene methyl t-butyldimethylsilyl acetal, Ketene tert-butyldimethylsilyl methyl acetal, tert-Butyl[(1-methoxyvinyl)oxy]dimethylsilane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)3CSi(CH3)2OC(OCH3)=CH2
CAS Number:
77086-38-5
Molecular Weight:
188.34
MDL number:
MFCD02683524
UNSPSC Code:
12352100
PubChem Substance ID:
24874073
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.429 (lit.)

bp

62 °C/9 mmHg (lit.)

density

0.863 g/mL at 25 °C (lit.)

SMILES string

COC(=C)O[Si](C)(C)C(C)(C)C

InChI

1S/C9H20O2Si/c1-8(10-5)11-12(6,7)9(2,3)4/h1H2,2-7H3

InChI key

UVCCWXJGWMGZAB-UHFFFAOYSA-N

Related Categories

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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.

Visit the Document Library

Enantioselective addition of ketene silyl acetals to nitrones catalyzed by chiral titanium complexes. Synthesis of optically active ?-amino acids.
Murahashi SI, et al.
Journal of the American Chemical Society, 124(12), 2888-2889 (2002)
New indenyl phosphinooxazoline complexes of iron and their catalytic activity in the Mukaiyama aldol reaction.
Lenze M, et al.
Tetrahedron Letters, 51(21), 2855-2858 (2010)
Three-step assembly of 4-aminotetrahydropyran-2-ones from isoxazoline-2-oxides.
Naumova AS, et al.
Royal Society of Chemistry Advances, 4(24), 12467-12475 (2014)
Recent developments in the syntheses of the epothilones and related analogues.
Watkins EB, et al.
European Journal of Organic Chemistry, 18, 4071-4084 (2006)

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