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| | Isopropyl ferulate Basic information |
| Product Name: | Isopropyl ferulate | | Synonyms: | TRANS-ISOPROPYL FERULATE;PROPAN-2-YL (E)-3-(4-HYDROXY-3-METHOXY-PHENYL)PROP-2-ENOATE;trans-Isopropyl;Isopropyl ferulate;3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid 1-methylethyl ester;4-Hydroxy-3-methoxycinnamic acid isopropyl ester;Isopropyl 3-(4-hydroxy-3-Methoxyphenyl)acrylate;iso-proylFerulic acid | | CAS: | 59831-94-6 | | MF: | C13H16O4 | | MW: | 236.26 | | EINECS: | | | Product Categories: | | | Mol File: | 59831-94-6.mol |  |
| | Isopropyl ferulate Chemical Properties |
| Boiling point | 358.2±27.0 °C(Predicted) | | density | 1.145±0.06 g/cm3(Predicted) | | pka | 8?+-.0.20(Predicted) | | form | Solid | | color | White to off-white |
| | Isopropyl ferulate Usage And Synthesis |
| 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 |
| | Isopropyl ferulate Preparation Products And Raw materials |
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