Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H12O3Si |
| Molecular Weight | 148.2325 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[Si](OC)(OC)C=C
InChI
InChIKey=NKSJNEHGWDZZQF-UHFFFAOYSA-N
InChI=1S/C5H12O3Si/c1-5-9(6-2,7-3)8-4/h5H,1H2,2-4H3
| Molecular Formula | C5H12O3Si |
| Molecular Weight | 148.2325 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Alkoxy/siloxy group exchange in the system vinyltrialkoxysilane-iridium(I) siloxide complex. | 2003 Jan 7 |
|
| Coupling of HDPE/hydroxyapatite composites by silane-based methodologies. | 2003 Jun |
|
| A novel carbon electrode material for highly improved EDLC performance. | 2006 Apr 20 |
|
| Tailoring elastic properties of silica aerogels cross-linked with polystyrene. | 2009 Mar |
|
| Improvement of catalytic properties of lipase from Arthrobacter sp. by encapsulation in hydrophobic sol-gel materials. | 2009 Oct |
|
| Efficient dielectrophoretic patterning of embryonic stem cells in energy landscapes defined by hydrogel geometries. | 2010 Dec |
|
| Terminal-vinyl liquid crystal crown ether-modified, vinyl-functionalized hybrid silica monolith for capillary electrochromatography. | 2010 Jun |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 06:42:34 GMT 2023
by
admin
on
Sat Dec 16 06:42:34 GMT 2023
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| Record UNII |
0ZIU135UES
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| Record Status |
Validated (UNII)
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| Record Version |
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76004
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0ZIU135UES
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220-449-8
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DTXSID2029240
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2768-02-7
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admin on Sat Dec 16 06:42:34 GMT 2023 , Edited by admin on Sat Dec 16 06:42:34 GMT 2023
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