The carbon atoms in the chemical structure of CINNAMIC ACID are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide … The molecular formula of CINNAMIC ACID is available in chemical formula page of CINNAMIC ACID, which identifies each constituent element by its chemical symbol and indicates the proportionate number of atoms of each element. trans-Cinnamic acid Description These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. Author(s):Marcin Mielecki and Bogdan Lesyng. c1ccc(cc1)/C=C/C(=O)O (trans)-Cinnamic Acid Compound with free spectra: 46 NMR, 14 FTIR, 2 Raman, 2 UV-Vis, and 23 MS It has a role as a plant metabolite. It is a white crystalline compound that is slightly soluble in water, and freely soluble in … Cinnamic acid exists as trans and cis isomers, but the trans form is the one most often found in nature and is the article of commerce. trans-Cinnamic acid. 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. Heat of Vaporization at Normal Boiling Point, LogP (Octanol-Water Partition Coefficient), Ghose-Crippen Octanol-Water Partition Coefficient (logP), Moriguchi Octanol-Water Partition Coefficient (logP), Activity Score for Ion Channel Modulators, Activity Score for Nuclear Receptor Ligands, Structure Data File (SDF/MOL File) of CINNAMIC ACID, download in the SDF page of CINNAMIC ACID, InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+, 19 atom(s) - 8 Hydrogen atom(s), 9 Carbon atom(s) and 2 Oxygen atom(s), 19 bond(s) - 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), Cinnamic acid, United States Pharmacopeia (USP) Reference Standard, trans-Cinnamic acid, natural, >=99%, FCC, FG. Sorry this one is long. It was first isolated in 1872 by F. Beilstein (of Handbook of Organic Chemistry fame) and A. Kuhlberg. View the Full Spectrum for FREE! Molecular Formula C 9 H 8 O 2; Average mass 148.159 Da; Monoisotopic mass 148.052429 Da; ChemSpider ID 392447 Hydroxycinnamic acids (hydroxycinnamates) are a class of aromatic acids or phenylpropanoids having a C 6 –C 3 skeleton. MDL number MFCD00004369. 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•. Articles of trans-Cinnamic acid are included as well. It is a crystalline compound that is white in colour and is slightly soluble in water. C&L Inventory 5 / 14. Differential scanning calorimetry showed that 1 undergoes a single fully reversible temperature induced phase transition at around 132/131 K (cooling/heating). Cinnamic acid is a white crystalline compound this is slightly soluble in water, or freely soluble in many organic solvents. 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. trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. Users can perform simple and advanced searches based on annotations relating to sequence, structure and function. 106.12 g of Benzaldehyde yields Cinnamic Acid = 148.16 g. 10.5 g of Benzaldehyde shall yield Cinnamic Acid = 148. Cinnamic acid exists as trans and cis isomers, but the trans form is the one most often found in nature and is the article of commerce. Author(s):Marcin Mielecki and Bogdan Lesyng. Cinnamic acid is an organic compound with the formula C 6 H 5 CH=CHCOOH. 12 x 10. Uses advised against Food, drug, pesticide or biocidal product use. Structure Identification: Photochem Photobiol Sci. The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. Molecular Weight 148.16 . The crystal structures of p-chloro-trans-cinnamic acid (I) and β-(p-chlorophenyl) propionic acid (II) have been determined from X-ray diffractometer data. Basic structure of quinic acid, chlorogenic acid, and typical hydroxycinnamate substituents. SAFETY DATA SHEET Creation Date 26-Sep-2009 Revision Date 14-Feb-2020 Revision Number 2 1. The couples of compounds differed for the kind of aromatic substitution (p-hydroxy, p-hydroxymethoxy, p-hydroxydimethoxy, dihydroxy). 16 / 106. At last,trans-Cinnamic acid… 2008 Sep;7(9):1063-70. 1999 Apr;47(4) :1453-9. Difference spectra in the FT-Raman amide I band depicted changes in the secondary structure of gluten network modified by five phenolic acids in the content 0.05%, 0.1% and 0.2%: cinnamic acid (CINA), coumaric acid (COUA), caffeic acid (CAFA), ferulic acid (FERA) and chlorogenic acid (CHLA). Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. It is found in Cinnamomum cassia. … Structure−activity relationship was derived also. Doceri is free in the iTunes app store. The full spectrum can only be viewed using a FREE account. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. In our definition, CGAs are all hydroxycinnamate esters of (−)-quinic acid. You can also browse global suppliers,vendor,prices,Price,manufacturers of trans-Cinnamic acid(140-10-3). (trans)-Cinnamic Acid Compound with free spectra: 46 NMR, 14 FTIR, 2 Raman, 2 UV-Vis, and 23 MS IUPAC names (2E)-3-phenylprop-2-enoic acid . ... cinnamic acid . 1c), 4‐hydroxycinnamic acid (p‐coumaric acid, Fig. … Learn more at http://www.doceri.com Linear Formula C 6 H 5 CH=CHCOOH . Beilstein/REAXYS Number 1905952 . 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. Molecular Weight. trans-Cinnamic acid is a sweet, balsam, and cinnamon tasting compound. Incompatible with strong oxidizing agents. Structure, properties, spectra, suppliers and links for: Cinnamic acid, m-hydroxy-, methyl ester. Affiliation:Bioinformatics Laboratory, Mossakowski Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, 02-106 Warsaw, Poland. Need to identify active compounds in your natural products? Structure, properties, spectra, suppliers and links for: Cinnamic acid, m-hydroxy-, methyl ester. 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. Molecular Weight 148.16 . CopyCopied, WBYWAXJHAXSJNI-VOTSOKGWSA-N Date s. Modify. In this study, we study the effect of the ethanol extract of C. cassia (CCE) and its active compound CA, on angiogenic processes in in vitro and in vivo. CopyCopied, InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+ 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). The first step has multiple possibilities. Naturally occurring compounds from this group include, among others: cinnamic acid, cinnamaldehyde (Fig. MDL number MFCD00004369. The contents of this page can freely be shared if cited as follows: Cinnamic acid structure. Shea, research. Then, try SnaPeaks – simply upload your MS/MS data and SnaPeaks will provide what’s in your natural products. 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). Almost all of the compounds showed some inhibition activity on each of the fungi at 0.5 mM. 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. 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. : A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid; trans-3-Phenylacrylic acid Recommended Use Laboratory chemicals. Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. A structure-antifungal activity relationship (SAR) study of 22 related cinnamic acid derivatives was carried out. Please hyperlink "Mol-Instincts" to www.molinstincts.com. Cinnamic acid is an organic compound with the formula C₆H₅CH=CHCOOH. Cinnamic acid is a naturally occurring aromatic acid and is considered to be safe for human consumption. Cinnamic acid structure. α-Cyano-4-hydroxycinnamic acid; Caffeic acid – burdock, hawthorn, artichoke, pear, basil, thyme, oregano, apple Cinnamic acid (CA) and its hydroxy-derivatives are aromatic building blocks whose structural peculiarities (unsaturation, hydroxylic and/or carboxylic groups) have driven them to a prominent position in polymer science. Attention was focused on the antifungal activities exhibited against Aspergillus flavus, Aspergillus terreus, and Aspergillus niger. 2005-03-26. Cinnamic acid is a white crystalline acid with a molecular formula C 9 H 8 O 2. Syntheses of the cis-cinnamic acid analogues 4–8: (a) ethyl 2-[bis(2-isopropylphenoxy)phosphoryl]acetate, Triton B, THF, −78 °C, 94%, Z:E = 98:2, (b) 10% NaOH aq., EtOH, rt, 97%, (c) MOMCl, diisopropylethylamine, 0 °C, 99%, (d) 2-cyanoethanol, EDCI, DMAP, CH 2 Cl 2, 0 °C, 91%, Z:E = 63:37, (e) (COCl) 2, DMF (1 drop), CH 2 Cl 2, 0 °C, (f) 28% NH 4 OH aq., CH 2 Cl 2, 0 °C, … 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. 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. Trans-3-phenyl-2-propenoic acid (cinnamic acid) derivatives: structure-activity relationship as hepatoprotective agents Medicinal chemistry (Shāriqah (United Arab Emirates)), 2007 Rosa Bobadilla 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. Beilstein/REAXYS Number 1905952 . 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. © 2020 ChemEssen, Inc. All rights reserved. A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. Mouse wheel zoom is available as well – the size of the CINNAMIC ACID molecule can be increased or decreased by scrolling the mouse wheel. UnitPot is a noteworthy web-based scientific unit converter that comes with an intuitive user interface. 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. EC Number 205-398-1. 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. EC Number 205-398-1. The carbon atoms in the chemical structure of CINNAMIC ACID are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide the carbon atom with four bonds. At last,trans-Cinnamic acid… Title:Cinnamic Acid Derivatives as Inhibitors of Oncogenic Protein Kinases – Structure, Mechanisms and Biomedical Effects# VOLUME: 23 ISSUE: 10. It is collected from the oil of cinnamon and is also found in shea butter. Doceri is free in the iTunes app store. The structure data file (SDF/MOL File) of CINNAMIC ACID is available for download in the SDF page of CINNAMIC ACID, which provides the information about the atoms, bonds, connectivity and coordinates of CINNAMIC ACID. 5 / 14. The observed fundamental frequencies (IR and Raman) were assigned according to their Royalty-Free Illustration. It is found in Cinnamomum cassia. Articles of trans-Cinnamic acid are included as well. It is a member of styrenes and a member of cinnamic acids. The first step has multiple possibilities. This video screencast was created with Doceri on an iPad. These molecules are visualized, downloaded, and analyzed by users who range from students to specialized scientists. 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. The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. The CINNAMIC ACID structure data file can be imported to most of the cheminformatics software systems and applications. The molecular structure is based on structures generated from information available in ECHA’s databases. Using a FREE account clicking and moving the mouse button also browse global suppliers,,. Revision Number 2 1 ) study of 22 related cinnamic acid is an organic compound with activity. Reaction vessel holds a colourless solution and bovine serum albumin as a member of cinnamic acid Supplementary Material Experimental this. Acid derivatives cinnamic acid structure Antioxidants: Structure-Activity Relation J Agric Food Chem = 148.16 10.5. 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