MDL number MFCD00004369. Date s. Modify. Structure, properties, spectra, suppliers and links for: Cinnamic acid, m-hydroxy-, methyl ester. Create. Molecular Weight. It is a member of styrenes and a member of cinnamic acids. [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 … Attention was focused on the antifungal activities exhibited against Aspergillus flavus, Aspergillus terreus, and Aspergillus niger. EC Number 205-398-1. 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 exists in all living species, ranging from bacteria to humans. 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. Cinnamic acid is an organic compound with the formula C6H5CHCHCO2H. 148.16 g/mol. 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. Fluorimetric studies on the binding of 4-(dimethylamino)cinnamic acid with micelles and bovine serum albumin. 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. It has a role as a plant metabolite. Introduction. Ultraviolet absorption spectra are recorded of cis‐ and trans‐ cinnamic acid, of cis‐ and trans‐1,2,3,4,‐tetrahydronaphthylidene (1) acetic acid and of cis‐ and trans‐β‐(naphthyl‐1) acrylic acid.The cis isomers all show a lower extinction coefficient and a shift of the maximum of absorption to shorter wave‐length in comparison with the trans isomers. Doceri is free in the iTunes app store. The crystal structure of trans-4-(trifluoromethyl) cinnamic acid (1) has been determined in the triclinic space groupP. trans-Cinnamic acid is a sweet, balsam, and cinnamon tasting compound. 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. 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. 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. Cinnamic acid structure. CGAs are ubiquitous in the plant kingdom, produced by nearly all plant species in variable amounts and with variable structures. Below are the list of the other names (synonyms) of CINNAMIC ACID including the various registry numbers, if available: Visit ChemTopia for further professional chemical information on the basis of a comprehensive intelligence networking platform for experts in the discipline around the globe. Hydroxycinnamic acids (hydroxycinnamates) are a class of aromatic acids or phenylpropanoids having a C 6 –C 3 skeleton. Cinnamic acid is a white crystalline acid with a molecular formula C 9 H 8 O 2. 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. Author(s):Marcin Mielecki and Bogdan Lesyng. 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. 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 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). It is found in Cinnamomum cassia. Details of the supplier of the safety data sheet Other (E)-3-phenylprop-2-enoic acid . Download preview. 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 2005-03-26. 2008 Sep;7(9):1063-70. SAFETY DATA SHEET Creation Date 26-Sep-2009 Revision Date 14-Feb-2020 Revision Number 2 1. It is found in Cinnamomum cassia. 106.12 g of Benzaldehyde yields Cinnamic Acid = 148.16 g. 10.5 g of Benzaldehyde shall yield Cinnamic Acid = 148. Stable. A structure-antifungal activity relationship (SAR) study of 22 related cinnamic acid derivatives was carried out. The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. cis-ferulic acid (CHEBI:76117) has functional parent cis-cinnamic acid (CHEBI:35699) cis-cinnamate (CHEBI:35700) is conjugate base of cis-cinnamic acid (CHEBI:35699) IUPAC Name (2 Z )-3-phenylprop-2-enoic acid Micelles and bovine serum albumin longer sophisticated with the formula C 6 H 5.... 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