| Identification | More | [Name]
TRANS-2-UNDECENAL | [CAS]
53448-07-0 | [Synonyms]
2-UNDECEN-1-AL
2-UNDECENAL
FEMA 3423
TRANS-2-HENDECEN-1-AL
TRANS-2-UNDECEN-1-AL
TRANS-2-UNDECEN-1-YL ALDEHYDE
TRANS-2-UNDECENAL
(2E)-2-Undecenal
(E)-2-Undecanal
(E)-2-undecenal
(E)-undec-2-enal
2-Undecenal, (E)-
2-Undecenal, trans
trans Undec-2-enal
undec-2(E)-enal
ETHYL UNDECANOATE 97+%
(E)-2-undecenal,trans-2-undecenal,(2E)-2-undecenal
trans-2-Undecenal, 95%, remainder mainly cis-isomer
trans-2-Hendecenal
trans-2-Undecenyl aldehyde | [EINECS(EC#)]
219-564-6 | [Molecular Formula]
C11H20O | [MDL Number]
MFCD00014680 | [Molecular Weight]
168.28 | [MOL File]
53448-07-0.mol |
| Hazard Information | Back Directory | [Definition]
ChEBI: A 2-undecenal in which the C2C bond has E configuration. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 52, p. 3558, 1987 DOI: 10.1021/jo00392a011
Tetrahedron Letters, 16, p. 1007, 1975 DOI: 10.1016/S0040-4039(00)72629-3 | [General Description]
trans-2-undecenal is mainly formed due to the oxidation of triolein while heating. It occurs naturally in coriander, fresh red pepper and watermelon. |
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