Other grades of this product :
| FARNESAL Basic information |
| Product Name: | FARNESAL | | Synonyms: | 10-dodecatrienal,3,7,11-trimethyl-6;3,7,11-trimethyl-dodeca-2,6,10-trienal;6,10-Dodecatrienal,3,7,11-trimethyl-2;farnesal,mixtureofisomers;TIMTEC-BB SBB007716;FARNESAL;FARNESONE;3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL | | CAS: | 19317-11-4 | | MF: | C15H24O | | MW: | 220.35 | | EINECS: | 242-957-9 | | Product Categories: | | Mol File: | 19317-11-4.mol |
| FARNESAL Chemical Properties |
| Boiling point | 126-129 °C3.5 mm Hg(lit.) | | density | 0.909 g/mL at 25 °C(lit.) | | FEMA | 4019 | 3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL | | refractive index | n20/D >1.4920(lit.) | | Fp | >230 °F | | storage temp. | Amber Vial, Refrigerator | | solubility | Chloroform (Sparingly), Methanol (Sparingly) | | form | Oil | | color | Pale Yellow to Yellow | | JECFA Number | 1228 | | BRN | 1723427 | | Stability: | Light Sensitive | | EPA Substance Registry System | 2,6,10-Dodecatrienal, 3,7,11-trimethyl- (19317-11-4) |
| FARNESAL Usage And Synthesis |
| Occurrence | Reportedly present in tomato, ginger and cardamom. | | Uses | Farnesone is s useful building block for organic synthesis | | Uses | Farnesal was used in the synthesis of sesquiterpene nanaimoal. | | Preparation | Reportedly prepared in a patented process by reaction of farnesol with diethyl ether in the presence of a catalyst. | | Synthesis Reference(s) | Synthetic Communications, 20, p. 3125, 1990 DOI: 10.1080/00397919008051535 | | General Description | Farnesal has been reported as specific lipid substrate for aldo-keto reductase 1B10 (AKR1B10). The incubation of farnesol with the protoplast of Botryococcus braunii B race strain leads to the formation of farnesal and 3-hydroxy-2,3-dihydrofarnesal. |
| FARNESAL Preparation Products And Raw materials |
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