Фенилуксусный альдегид
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Фенилуксусный альдегид
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. Phenylacetaldehyde occurs extensively in nature because it can be biosynthetically derived from the amino acid phenylalanine. Natural sources of the compound include chocolate , \\\\\\\\\\\\[2\\\\\\\\\\\\] buckwheat , \\\\\\\\\\\\[3\\\\\\\\\\\\] flowers , and communication pheromones from various insect orders. The aroma of pure substance can be described as honey-like, sweet, rose, green, grassy and is added to fragrances to impart hyacinth , narcissi , or rose nuances. Historically, before biotechnology approaches were developed, phenylacetaldehyde was also used to produce phenylalanine via the Strecker reaction as a step in the production of aspartame sweetener. Phenylacetaldehyde is used in the synthesis of polyesters where it serves as a rate-controlling additive during polymerization. Phenylacetaldehyde is responsible for the antibiotic activity of maggot therapy. Theoretically, hydrazone formation and subsequent reduction of the phenylethylidenehydrazine gives phenelzine. Phenylacetaldehyde can be obtained via various synthetic routes and precursors. Notable examples include:. Phenylacetaldehyde is often contaminated with polystyrene oxide polymer because of the especial lability of the benzylic alpha proton and the reactivity of the aldehyde. Aldol condensation of the initial dimer gives rise to a range of Michael acceptors and donors. From Wikipedia, the free encyclopedia. CAS Number. Interactive image. Beilstein Reference. PubChem CID. Chemical formula. Solubility in water. Refractive index n D. Journal of Agricultural and Food Chemistry. Food Chemistry. Extensive Database of Insect Pheromones and Semiochemicals. Retrieved 26 November Environmental Entomology. Justus Liebigs Annalen der Chemie. Newyork: John Wiley and Sons Inc. Retrieved 15 June Chemical Reviews. Categories : Insect pheromones Aldehydes Phenyl compounds. Namespaces Article Talk. Views Read Edit View history. By using this site, you agree to the Terms of Use and Privacy Policy. Other names 2-Phenylacetaldehyde Hyacinthin Phenylethanal. Main hazards. R-phrases outdated. R22 R36 R37 R S-phrases outdated. S26 S
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Фенилуксусный альдегид
Ацетальдегид
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. Phenylacetaldehyde occurs extensively in nature because it can be biosynthetically derived from the amino acid phenylalanine. Natural sources of the compound include chocolate , \\\\\\\\\\\\\\[2\\\\\\\\\\\\\\] buckwheat , \\\\\\\\\\\\\\[3\\\\\\\\\\\\\\] flowers , and communication pheromones from various insect orders. The aroma of pure substance can be described as honey-like, sweet, rose, green, grassy and is added to fragrances to impart hyacinth , narcissi , or rose nuances. Historically, before biotechnology approaches were developed, phenylacetaldehyde was also used to produce phenylalanine via the Strecker reaction as a step in the production of aspartame sweetener. Phenylacetaldehyde is used in the synthesis of polyesters where it serves as a rate-controlling additive during polymerization. Phenylacetaldehyde is responsible for the antibiotic activity of maggot therapy. Theoretically, hydrazone formation and subsequent reduction of the phenylethylidenehydrazine gives phenelzine. Phenylacetaldehyde can be obtained via various synthetic routes and precursors. Notable examples include:. Phenylacetaldehyde is often contaminated with polystyrene oxide polymer because of the especial lability of the benzylic alpha proton and the reactivity of the aldehyde. Aldol condensation of the initial dimer gives rise to a range of Michael acceptors and donors. From Wikipedia, the free encyclopedia. CAS Number. Interactive image. Beilstein Reference. PubChem CID. Chemical formula. Solubility in water. Refractive index n D. Journal of Agricultural and Food Chemistry. Food Chemistry. Extensive Database of Insect Pheromones and Semiochemicals. Retrieved 26 November Environmental Entomology. Justus Liebigs Annalen der Chemie. Newyork: John Wiley and Sons Inc. Retrieved 15 June Chemical Reviews. Categories : Insect pheromones Aldehydes Phenyl compounds. Namespaces Article Talk. Views Read Edit View history. By using this site, you agree to the Terms of Use and Privacy Policy. Other names 2-Phenylacetaldehyde Hyacinthin Phenylethanal. Main hazards. R-phrases outdated. R22 R36 R37 R S-phrases outdated. S26 S
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