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Learn more at http://www.doceri.com It is a conjugate acid of a cinnamate. 25 matches found for trans-cinnamic acid Advanced Search | Structure Search Sort By Relevance Name ↑ Name ↓ Base Name ↑ Base Name ↓ Formula Weight ↑ Formula Weight ↓ For physicochemical, thermodynamic, transport, spectra, and other property data & information, the followings are available from “Mol-Instincts”, a chemical database based on quantum mechanics: The SMILES string of CINNAMIC ACID is OC(=O)C=Cc1ccccc1, which can be can be imported by most molecule editors for conversion back into two-dimensional drawings or three-dimensional models of the CINNAMIC ACID. 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. trans-Cinnamic acid is a weakly acidic compound (based on its pKa). It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. c1ccc(cc1)/C=C/C(=O)O Royalty-Free Illustration. Cinnamic acid structure. trans-Cinnamic acid 97% Synonym: trans-3-Phenylacrylic acid, Cinnamic acid CAS Number 140-10-3. 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. 5 / 14. Linear Formula C 6 H 5 CH=CHCOOH . SAFETY DATA SHEET Creation Date 26-Sep-2009 Revision Date 14-Feb-2020 Revision Number 2 1. [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 … Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. … (trans)-Cinnamic Acid Compound with free spectra: 46 NMR, 14 FTIR, 2 Raman, 2 UV-Vis, and 23 MS The first step has multiple possibilities. Author(s):Marcin Mielecki and Bogdan Lesyng. Introduction. Beilstein/REAXYS Number 1905952 . trans-Cinnamic acid Description These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. The CINNAMIC ACID compound may be called differently depending on the various different situations of industrial applications. The information of the atoms, bonds, connectivity and coordinates included in the chemical structure of CINNAMIC ACID can easily be identified by this visualization. trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. Images of the chemical structure of CINNAMIC ACID are given below: The 2D chemical structure image of CINNAMIC ACID is also called skeletal formula, which is the standard notation for organic molecules. It is a white crystalline compound that is slightly soluble in water, and freely soluble in … ... cinnamic acid . 12 x 10. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. 5 = 14.66 g. Hence, Theoretical yield of Cinnamic Acid = 14.66 g. If reported Practical yield = 9.5 g. Then, Percentage Practical yield = Practical yield / Theoretical yield × 100 = 9. 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. In our definition, CGAs are all hydroxycinnamate esters of (−)-quinic acid. Cinnamic acid is an organic compound with the formula C 6 H 5 CH=CHCOOH. The CINNAMIC ACID molecule shown in the visualization screen can be rotated interactively by keep clicking and moving the mouse button. 1a) and its simple derivatives are widely represented in plants. Hydroxycinnamic acids (hydroxycinnamates) are a class of aromatic acids or phenylpropanoids having a C 6 –C 3 skeleton. Cinnamic acid is an organic compound with the formula C₆H₅CH=CHCOOH. It exists as both a cis and a trans isomer, although the latter is more common. trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. A monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. It was first isolated in 1872 by F. Beilstein (of Handbook of Organic Chemistry fame) and A. Kuhlberg. MDL number MFCD00004369. Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. The 3D chemical structure image of CINNAMIC ACID is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them. These compounds are hydroxy derivatives of cinnamic acid.. The crystal structure of trans-4-(trifluoromethyl) cinnamic acid (1) has been determined in the triclinic space groupP. CopyCopied, CSID:392447, http://www.chemspider.com/Chemical-Structure.392447.html (accessed 23:29, Jan 8, 2021) 709 View the Full Spectrum for FREE! For a better understanding of the chemical structure, an interactive 3D visualization of CINNAMIC ACID is provided here. The E (trans) isomer of cinnamic acid. 16 / 106. Details of the supplier of the safety data sheet Fluorimetric studies on the binding of 4-(dimethylamino)cinnamic acid with micelles and bovine serum albumin. 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. Visit ChemicalBook To find more trans-Cinnamic acid(140-10-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. Stereoisomers: (Z)-3-Phenyl-2-propenoic acid; 2-Propenoic acid, 3-phenyl- 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 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 . CopyCopied, InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+ You can also browse global suppliers,vendor,prices,Price,manufacturers of trans-Cinnamic acid(140-10-3). Source: Mol-Instincts Chemical Database, Predicted on Quantum. CGAs are ubiquitous in the plant kingdom, produced by nearly all plant species in variable amounts and with variable structures. Incompatible with strong oxidizing agents. trans-Cinnamic acid is a sweet, balsam, and cinnamon tasting compound. Uses advised against Food, drug, pesticide or biocidal product use. 1b), cinnamyl alcohol (Fig. It is obtained from cinnamon bark and balsam resins such as storax. Cinnamic acid is a white crystalline compound this is slightly soluble in … The contents of this page can freely be shared if cited as follows: Attention was focused on the antifungal activities exhibited against Aspergillus flavus, Aspergillus terreus, and Aspergillus niger. This video screencast was created with Doceri on an iPad. 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. 16 / 106. α-Cyano-4-hydroxycinnamic acid; Caffeic acid – burdock, hawthorn, artichoke, pear, basil, thyme, oregano, apple Almost all of the compounds showed some inhibition activity on each of the fungi at 0.5 mM. Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. 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 molecule contains a total of 19 bond(s) There are 11 non-H bond(s), 8 multiple bond(s), 2 rotatable bond(s), 2 double bond(s), 6 aromatic bond(s), 1 six-membered ring(s), 1 carboxylic acid(s) (aliphatic) and 1 hydroxyl group(s). 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. Basic structure of quinic acid, chlorogenic acid, and typical hydroxycinnamate substituents. Visit ChemicalBook To find more trans-Cinnamic acid(140-10-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. … The antioxidant activity of selected representatives of flavonoids, coumarins, and cinnamic acids was examined by measuring their protective action toward linoleic acid peroxidation in micelles of sodium dodecyl sulfate in buffer solution, pH 7.4. Cinnamic acid structure. 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 CopyCopied, Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, Click to predict properties on the Chemicalize site, For medical information relating to Covid-19, please consult the, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:27386, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:35697, ACD/Labs Percepta Platform - PhysChem Module, US Environmental Protection Agency’s EPISuite™, Compounds with the same molecular formula, Search Google for structures with same skeleton, 147 deg C / 4 mm (350.4434 °C / 760 mmHg). Sorry this one is long. Cinnamic acid is a white crystalline compound this is slightly soluble in water, or freely soluble in many organic solvents. In the category of phytochemicals that can be found in food, there are : . Cinnamic acid is an organic compound with the formula C6H5CHCHCO2H. Pre-Registration process . After the addition of bromine to trans-cinnamic acid, the product was identified by its melting point and infrared spectrum resulting in erythro-2,3-Dibromo-3-phenylpropanoic acid after comparing similar properties. Users can perform simple and advanced searches based on annotations relating to sequence, structure and function. Attention was focused on the antifungal activities exhibited against Aspergillus flavus, Aspergillus terreus, and Aspergillus niger. Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. UnitPot is a noteworthy web-based scientific unit converter that comes with an intuitive user interface. 2020-12-26. Download preview. trans-Cinnamic acid ≥99% Synonym: trans-3-Phenylacrylic acid, Cinnamic acid CAS Number 140-10-3. Date s. Modify. 5 / 14. Cinnamic acid is a naturally occurring aromatic acid and is considered to be safe for human consumption. Cinnamic acid is a white crystalline acid with a molecular formula C 9 H 8 O 2. Cinnamic acid molecular structure isolated on white. Indeed, CA hydroxy-derivatives (hydroxycinnamic acids, … EC Number 205-398-1. Cinnamic acid is an organic compound with the formula C6H5CH=CHCOOH. Structure−activity relationship was derived also. Cinnamic acid. 2008 Sep;7(9):1063-70. Bromination of Cinnamic acid Supplementary Material Experimental notes This experiment aims at the preparation of the 2,3-dibromo-3-phenylpropanoic acid from cinnamic acid by bromine addition. Molecular Weight. 140-10-3 - WBYWAXJHAXSJNI-VOTSOKGWSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. In this present study, FT-IR, FT-Raman, (13)C NMR and (1)H NMR spectra for cinnamic acid have been recorded for the vibrational and spectroscopic analysis. 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