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| | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate Basic information |
| Product Name: | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate | | Synonyms: | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate;Benzoic acid, 2-2-methyl-3-4-(1-methylethyl)phenylpropylideneamino-, methyl ester;CYCLAMENALDEHYDEMETHYLANTHRANILATE;Cyclamen aldehyde-methyl anthranilate (Schiff base);Methyl-2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propyliden]amino]benzoat;2-((2-Methyl-3-(4-(1-methylethyl)phenyl)propylidene)amino)benzoic acid, methyl ester;Einecs 202-072-0;Cyclantine | | CAS: | 91-50-9 | | MF: | C21H25NO2 | | MW: | 323.43 | | EINECS: | 202-072-0 | | Product Categories: | | | Mol File: | 91-50-9.mol | ![methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate Structure](CAS/GIF/91-50-9.gif) |
| | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate Chemical Properties |
| | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate Usage And Synthesis |
| Chemical Properties | Yellowish viscous liquid, barely pourable at room temperature. Almost insoluble in water and Propylene glycol. Soluble in alcohol and perfume oils. Intensely sweet, fresh-floral odor of great tenacity, somewhat reminiscent of the flowers of the Lemon tree. Greener and more diffusive than Hydroxycitronellal-Methylanthranilate. | | Uses | Finds some use in perfume compositions, probably ranking No. 3 among Schiff’s bases after Aurantiol and Acaciol. Its fresher odor type and less “Orangeblossom”’-character are its main assets. | | Synthesis | Methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate is prepared by condensation of Cyclamenaldehyde and Methylanthranilate. |
| | methyl 2-[[2-methyl-3-[4-(1-methylethyl)phenyl]propylidene]amino]benzoate Preparation Products And Raw materials |
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