cinnamic acid structure

Introduction. … Trans-3-phenyl-2-propenoic acid (cinnamic acid) derivatives: structure-activity relationship as hepatoprotective agents Medicinal chemistry (Shāriqah (United Arab Emirates)), 2007 Rosa Bobadilla The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. Linear Formula C 6 H 5 CH=CHCOOH . In the category of phytochemicals that can be found in food, there are : . Incompatible with strong oxidizing agents. C&L Inventory (E)-3-(4-methoxy-3-(3-methylbut-2-enyl)phenyl)acrylic … Cinnamic acid molecular structure isolated on white. The full spectrum can only be viewed using a FREE account. The kinetic behavior of cinnamic acids, their methyl esters, and two catechols 1−10 (ArOH) in the reaction with DPPH• in methanol and ethanol is not compatible with a reaction mechanism that involves hydrogen atom abstraction from the hydroxyl group of 1−10 by DPPH•. A series of cinnamic acid esters and their derivatives were synthesized and evaluated for antifungal activities in vitro against four plant pathogenic fungi by using the mycelium growth rate method. Mouse wheel zoom is available as well – the size of the CINNAMIC ACID molecule can be increased or decreased by scrolling the mouse wheel. However, relatively little work has been carried out on the angiogenic responses of C. cassia and its active compound cinnamic acid (CA), despite its excellent pharmacological action. 5 / 14. EC Number 205-398-1. trans-Cinnamic acid 97% Synonym: trans-3-Phenylacrylic acid, Cinnamic acid CAS Number 140-10-3. It is a crystalline compound that is white in colour and is slightly soluble in water. Beilstein/REAXYS Number 1905952 . Author(s):Marcin Mielecki and Bogdan Lesyng. It has a role as a plant metabolite. It was first isolated in 1872 by F. Beilstein (of Handbook of Organic Chemistry fame) and A. Kuhlberg. Data compiled as indicated in comments: ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein DH- Eugene S. Domalski and Elizabeth D. Hearing [Pubmed: 18754053] The constrained photophysics of intramolecular charge transfer (ICT) probe 4-(Dimethylamino)cinnamic acid (DMACA) was studied in different surfactant systems as well as in … Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Formula: C 9 H 8 O 2; Molecular weight: 148.1586; IUPAC Standard InChI: Classified as an unsaturated carboxylic acid, it occurs naturally in a number of plants.It exists as both a cis and a trans isomer, although the latter is more common. The observed fundamental frequencies (IR and Raman) were assigned according to their Uses advised against Food, drug, pesticide or biocidal product use. MDL number MFCD00004369. Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. CopyCopied, CSID:392447, http://www.chemspider.com/Chemical-Structure.392447.html (accessed 23:29, Jan 8, 2021) Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. Identification Product Name trans-Cinnamic acid Cat No. Benzoic and Cinnamic Acid Derivatives as Antioxidants: Structure-Activity Relation J Agric Food Chem. It is obtained from cinnamon bark and balsam resins such as storax. 5 / 14. Conversion of complicated chemical-related units is no longer sophisticated with the aid of UnitPot. The information of the atoms, bonds, connectivity and coordinates included in the chemical structure of CINNAMIC ACID can easily be identified by this visualization. The electronic absorption spectra of cinnamic acid and some cinnamoyl azides have been recorded in absolute methanol and investigated to explore the structure of the titled compounds. The radius of the spheres is therefore smaller than the rod lengths in order to provide a clearer view of the atoms and bonds throughout the chemical structure model of CINNAMIC ACID. 12 x 10. 16 / 106. Molecular Formula C 9 H 8 O 2; Average mass 148.159 Da; Monoisotopic mass 148.052429 Da; ChemSpider ID 392447 Differential scanning calorimetry showed that 1 undergoes a single fully reversible temperature induced phase transition at around 132/131 K (cooling/heating). 2008 Sep;7(9):1063-70. Structure Identification: Photochem Photobiol Sci. α-Cyano-4-hydroxycinnamic acid; Caffeic acid – burdock, hawthorn, artichoke, pear, basil, thyme, oregano, apple The E (trans) isomer of cinnamic acid. 106.12 g of Benzaldehyde yields Cinnamic Acid = 148.16 g. 10.5 g of Benzaldehyde shall yield Cinnamic Acid = 148. 1999 Apr;47(4) :1453-9. It is obtained from cinnamon bark and balsam resins such as storax. trans-Cinnamic acid is a weakly acidic compound (based on its pKa). A series of cinnamic acid derivatives, amides (1-12) and esters (13-22), were synthesized, and structure-activity relationships for antioxidant activity, and monoamine oxidases (MAO) A and B, acetylcholinesterase, and butyrylcholinesterase (BChE) inhibitory activities were analyzed. The CINNAMIC ACID compound may be called differently depending on the various different situations of industrial applications. 709 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. : A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid; trans-3-Phenylacrylic acid Recommended Use Laboratory chemicals. Organic Compound; Ester; Food Toxin; Plant Toxin; Metabolite; Household Toxin; Natural Compound, ORL-RAT LD50 2500 mg kg-1, IPR-RAT LD50 1600 mg kg-1, ORL-MUS LD50 5000 mg kg-1, IPR-MUS LD50 160 mg kg-1, P261; P280; P302+P352; P304+P340; P305+P351+P338; P312, WARNING: Irritates skin and eyes, harmful if swallowed. Organic compound with the activity of the chemical bonds that hold the atoms together at the 3-position the mouse.... 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