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Пиперональ вики
Piperonal , also known as heliotropin , is an organic compound which is commonly found in fragrances and flavors. Piperonal naturally occurs in various plants. Examples include dill , vanilla , violet flowers , and black pepper. Piperonal can be prepared by oxidizing isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene. Piperonal, like all aldehydes , can be reduced to its alcohol piperonyl alcohol or oxidized to give its acid piperonylic acid. Piperonal can be used in the synthesis of some pharmaceutical drugs including tadalafil , \\\\\\\\\\\\[6\\\\\\\\\\\\] L-DOPA , \\\\\\\\\\\\[7\\\\\\\\\\\\] and atrasentan. Piperonal has a floral odor which is commonly described as being similar to that of vanillin or cherry. For this reason it is commonly used in fragrances and artificial flavors. Piperonyl acetate is a synthetic cherry flavoring. From Wikipedia, the free encyclopedia. Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde;. CAS Number. Interactive image Interactive image. Chemical formula. Solubility in water. LD 50 median dose. Tetrahedron Letters. Journal of the Chemical Society 9 : — Organic Communications. Preparation of 3- 3, 4-Methylenedioxyphenyl -D-, and -L-alanine'. Discovery of A'. Journal of Medicinal Chemistry. Categories : Benzaldehydes Benzodioxoles. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy. Other names Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde;. Colorless crystals \\\\\\\\\\\\[1\\\\\\\\\\\\]. Soluble in parts \\\\\\\\\\\\[1\\\\\\\\\\\\]. Lethal dose or concentration LD, LC :.
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Пиперональ вики
Гелиотропин
Piperonal , also known as heliotropin , is an organic compound which is commonly found in fragrances and flavors. Piperonal naturally occurs in various plants. Examples include dill , vanilla , violet flowers , and black pepper. Piperonal can be prepared by oxidizing isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene. Piperonal, like all aldehydes , can be reduced to its alcohol piperonyl alcohol or oxidized to give its acid piperonylic acid. Piperonal can be used in the synthesis of some pharmaceutical drugs including tadalafil , \\\\\\\\\\\\\\[6\\\\\\\\\\\\\\] L-DOPA , \\\\\\\\\\\\\\[7\\\\\\\\\\\\\\] and atrasentan. Piperonal has a floral odor which is commonly described as being similar to that of vanillin or cherry. For this reason it is commonly used in fragrances and artificial flavors. Piperonyl acetate is a synthetic cherry flavoring. From Wikipedia, the free encyclopedia. Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde;. CAS Number. Interactive image Interactive image. Chemical formula. Solubility in water. LD 50 median dose. Tetrahedron Letters. Journal of the Chemical Society 9 : — Organic Communications. Preparation of 3- 3, 4-Methylenedioxyphenyl -D-, and -L-alanine'. Discovery of A'. Journal of Medicinal Chemistry. Categories : Benzaldehydes Benzodioxoles. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy. Other names Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde;. Colorless crystals \\\\\\\\\\\\\\[1\\\\\\\\\\\\\\]. Soluble in parts \\\\\\\\\\\\\\[1\\\\\\\\\\\\\\]. Lethal dose or concentration LD, LC :.
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