Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H16O2 |
| Molecular Weight | 156.2221 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCOC(=O)C=C
InChI
InChIKey=LNMQRPPRQDGUDR-UHFFFAOYSA-N
InChI=1S/C9H16O2/c1-3-5-6-7-8-11-9(10)4-2/h4H,2-3,5-8H2,1H3
| Molecular Formula | C9H16O2 |
| Molecular Weight | 156.2221 |
| 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 |
|---|---|---|
| Antimicrobial activity of p-hydroxyphenyl acrylate derivatives. | 2004 Dec 15 |
|
| Non-particulate (continuous bed or monolithic) acrylate-based capillary columns for reversed-phase liquid chromatography and electrochromatography. | 2005 Apr 15 |
|
| Tools for fluorescent molecularly imprinted polymers. | 2005 Jan 15 |
|
| Development of acrylate-based monolithic stationary phases for electrochromatographic separations. | 2005 Nov |
|
| Chemoselective alkylation of N-alkylaminooxy-containing peptides. | 2006 Aug 3 |
|
| Electrochromatography in poly(dimethyl)siloxane microchips using organic monolithic stationary phases. | 2007 Jun |
|
| Online preconcentration using monoliths in electrochromatography capillary format and microchips. | 2007 Nov |
|
| Alkyl chain length effects on copolymerization kinetics of a monoacrylate with hexanediol diacrylate. | 2007 Nov-Dec |
|
| Determination of trace levels of benzodiazepine in urine using capillary electrochromatography-time of flight mass spectrometry. | 2008 May |
|
| CEC separation of peptides using a poly(hexyl acrylate-co-1,4-butanediol diacrylate-co-[2-(acryloyloxy)ethyl]trimethyl ammonium chloride) monolithic column. | 2008 Sep |
|
| On the nature of ionic liquids and their effects on lipases that catalyze ester synthesis. | 2009 Mar 25 |
|
| Prediction of the reduced glutathione (GSH) reactivity of dental methacrylate monomers using NMR spectra - Relationship between toxicity and GSH reactivity. | 2009 Nov |
|
| Hydrophobically modified oligoethylenimines as highly efficient transfection agents for siRNA delivery. | 2009 Nov |
|
| The potential dermal irritating effect of residual (meth)acrylic monomers in pressure sensitive adhesive tapes. | 2010 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:51:09 GMT 2023
by
admin
on
Fri Dec 15 19:51:09 GMT 2023
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| Record UNII |
X0670P452A
|
| Record Status |
Validated (UNII)
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| Record Version |
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