Webtrans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 IUPAC Name: 3-phenylacrylic acid. Cinn Acid Tech State Form: other: Solid. Constituent 1. Reference substance name: trans-cinnamic acid EC Number: 205-398-1 EC Name: trans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 ... WebJan 10, 2024 · Chemsrc provides Cinnamic aldehyde(CAS#:14371-10-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of Cinnamic aldehyde are included as well. ... CAS REGISTRY NUMBER : 14371-10-9 BEILSTEIN REFERENCE NO. : 1071571 LAST UPDATED : 199712 DATA ITEMS CITED : 7 …
Cinnamaldehyde C9H8O Supreme Pharmatech
WebCinnamaldehyde C9H8O CID 637511 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety ... WebJan 3, 2024 · Chemsrc provides Cinnamic acid(CAS#:621-82-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of Cinnamic acid … csharp discord server
2-(2-Bromopropanoyl)-5-(cyanomethyl)cinnamic acid 1807435 …
WebGet all info about AMYL CINNAMAL, ingredient details containing - Uses, formulation, toxicity, and alternatives. Also, know supplier and product information ... CAS Number: … WebAldrich-C31600; 4-Chlorocinnamic acid 0.99; CAS No.: 1615-02-7; Synonyms: trans-3-(4-Chlorophenyl)propenoic acid; Linear Formula: ClC6H4CH=CHCO2H; Empirical Formula ... The biosynthesis of cinnamaldehyde begins with deamination of L-phenylalanine into cinnamic acid by the action of phenylalanine ammonia lyase (PAL). PAL catalyzes this reaction by a non-oxidative deamination. This deamination relies on the MIO prosthetic group of PAL. PAL gives rise to trans-cinnamic acid. See more Cinnamaldehyde is an organic compound with the formula() C6H5CH=CHCHO. Occurring naturally as predominantly the trans (E) isomer, it gives cinnamon its flavor and odor. It is a phenylpropanoid that is naturally … See more As a flavorant The most obvious application for cinnamaldehyde is as flavoring in chewing gum, ice cream, candy, e-liquid and beverages; … See more Cinnamaldehyde is used in agriculture because of its low toxicity, but it is a skin irritant. Cinnameldahyde may cause allergic contact stomatitis in sensitised individuals, however allergy to the compound is believed to be uncommon. See more • GMD MS Spectrum See more Cinnamaldehyde was isolated from cinnamon essential oil in 1834 by Jean-Baptiste Dumas and Eugène-Melchior Péligot and synthesized in the laboratory by the Italian chemist Luigi Chiozza in 1854. The natural product is See more Numerous derivatives of cinnamaldehyde are commercially useful. Dihydrocinnamyl alcohol (3-phenylpropanol) occurs naturally but is produced by double hydrogenation of … See more Cinnamaldehyde is a dietary antimutagen that effectively inhibits both induced and spontaneous mutations. Experimental evidence indicates … See more csharp dll 反编译