Phenol, 2-methoxy-4-(1-propenyl)-, (Z)-
- Formula: C10H12O2
- Molecular weight: 164.2011
- IUPAC Standard InChI: InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3-7,11H,1-2H3/b4-3-
- IUPAC Standard InChIKey: BJIOGJUNALELMI-ARJAWSKDSA-N
- CAS Registry Number: 5912-86-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Stereoisomers:
- Other names: Phenol, 2-methoxy-4-propenyl-, (Z)-; cis-Isoeugenol; cis-2-Methoxy-4-propenylphenol; Isoeugenol, Z-; 2-Methoxy-4-[(1Z)-1-propenyl]phenol; 4-(1-Propenyl)-2-methoxyphenol, (Z)-; (Z)-Isoeugenol; (Z)-2-Methoxy-4-(prop-1-enyl)phenol; cis-4-Propenylguaiacol; 1-(2-furanyl)-2-hydroxyethanone; (Z)-2-Methoxy-5-(1-propenyl)phenol
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Normal alkane RI, polar column, custom temperature program
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
| Column type | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|
| Active phase | Supelcowax-10 | FFAP | SOLGel-Wax | Carbowax 20M |
| Column length (m) | 30. | 30. | ||
| Carrier gas | Helium | Helium | Helium | |
| Substrate | ||||
| Column diameter (mm) | 0.25 | 0.53 | ||
| Phase thickness (μm) | 0.25 | 0.50 | ||
| Program | 45 0C 3 0C/min -> 230 0C (10 min) 10 0C/min -> 270 0C (21 min) | not specified | 40 0C 7 0C/min -> 180 0C 10 0C/min -> 240 0C (10 min) | not specified |
| I | 2226. | 2287. | 2240. | 2230. |
| Reference | de Simon, Estruelas, et al., 2009 | Frauendorfer and Schieberle, 2008 | Shu and Shen, 2008 | Vinogradov, 2004 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
References
Go To: Top, Normal alkane RI, polar column, custom temperature program, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
de Simon, Estruelas, et al., 2009
de Simon, B.F.; Estruelas, E.; Munoz, A.M.; Cadahia, E.; Sanz, M.,
Volatile compounds in acacia, chestnut, cherry, ash, and oak woods, with a view to their use in cooperage,
J. Agric. Food Chem., 2009, 57, 8, 3217-3227, https://doi.org/10.1021/jf803463h
. [all data]
Frauendorfer and Schieberle, 2008
Frauendorfer, F.; Schieberle, P.,
Changes in key aroma compounds of criollo cocoa beans during roasting,
J. Agric. Food Chem., 2008, 56, 21, 10244-10251, https://doi.org/10.1021/jf802098f
. [all data]
Shu and Shen, 2008
Shu, N.; Shen, H.,
Aroma-impact compounds in Lysimachia foenum-graecum extracts,
Flavour Fragr. J., 2008, 24, 1, 1-6, https://doi.org/10.1002/ffj.1908
. [all data]
Vinogradov, 2004
Vinogradov, B.A.,
Production, composition, properties and application of essential oils, 2004, retrieved from http://viness.narod.ru. [all data]
Notes
Go To: Top, Normal alkane RI, polar column, custom temperature program, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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