| Identification | Back Directory | [Name]
Isopropyl ferulate | [CAS]
59831-94-6 | [Synonyms]
trans-Isopropyl
Isopropyl ferulate
iso-proylFerulic acid
Ferulic Acid Impurity 4
TRANS-ISOPROPYL FERULATE
Isopropyl 3-(4-hydroxy-3-Methoxyphenyl)acrylate
4-Hydroxy-3-methoxycinnamic acid isopropyl ester
PROPAN-2-YL (E)-3-(4-HYDROXY-3-METHOXY-PHENYL)PROP-2-ENOATE
3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid 1-methylethyl ester
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, 1-methylethyl ester | [Molecular Formula]
C13H16O4 | [MDL Number]
MFCD01736873 | [MOL File]
59831-94-6.mol | [Molecular Weight]
236.26 |
| Chemical Properties | Back Directory | [Boiling point ]
358.2±27.0 °C(Predicted) | [density ]
1.145±0.06 g/cm3(Predicted) | [form ]
Solid | [pka]
8?+-.0.20(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
Isopropyl ferulate, isolated from Notopterygium incisum, is used in the reduction of pharmaceuticals, preparation of antifungal agents, cosmetics and as antioxidant agent and so forth[1]. | [References]
[1] Kumar A, et al. Synthesis of isopropyl ferulate using silica-immobilized lipase in an organic medium. Enzyme Res. 2011;2011:718949. DOI:10.4061/2011/718949
[2] Li F, et al. Anti-austerity agents from Rhizoma et Radix Notopterygii (Qianghuo). Planta Med. 2012 May;78(8):796-9. DOI:10.1055/s-0031-1298463 |
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