It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. 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. trans-Cinnamic acid is a weakly acidic compound (based on its pKa). Classified as an unsaturated carboxylic acid, it occurs naturally in a number of plants. trans-Cinnamic acid Description These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. CAS Number: 63938-16-9 . CINNAMIC ACID . IUPAC name of cinnamic acid => (2E)-3-Phenylprop-2-enoic acid. cinnamic acid: ChEBI ID CHEBI:27386: Definition A monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. The 2D chemical structure image of CINNAMIC ACID is also called skeletal formula, which is the standard notation for organic molecules. Watch Queue Queue. Uses of Methyl Cinnamate (Cinnamic acid methyl ester): ... Cinnamaldehyde, or 3-phenylprop-2-enal to use its IUPAC name, is a member of the class of compounds known as cinnamaldehydes. Type of substance Composition: mono-constituent substance Origin: organic Total tonnage band Total range: 10 - 100 tonnes per annum REACH Classified as an unsaturated carboxylic acid, it occurs naturally … CAS Number: 63938-16-9 . Identification Name 2,4-Dihydroxy-Trans Cinnamic Acid Accession Number DB01704 Description Not Available Type Small Molecule Groups Experimental Structure Slightly soluble in water. trans-Cinnamic acid is used in flavors, synthetic indigo and pharmaceuticals. EC number: 205-398-1 | CAS number: 140-10-3 . Cinnamic acid has the formula C6H5CHCHCOOH and is an odorless white crystalline acid, which is slightly soluble in water. Cinnamic Acid Cinnamic acid is a naturally-occurring, organic, unsaturated carboxylic acid that exists as both cis and trans isomers. Cinnamic acid is an organic compound with the formula C 6 H 5 CHCHCO 2 H. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. Its common name is cinnamic acid. From Wikipedia. Table 1 shows the abbreviated name, common- and IUPAC names and molar mass of CA derivatives used for … It also contains a phenyl group at third carbon atom. cinnamic acid, (Z)-isomer ... IUPAC Name: (E)-3-phenylprop-2-enoic acid . What is iupac name cinnamic acid Ask for details ; Follow Report by Chikky5555 01.01.2018 Log in to add a comment View our Cinnamic acids and derivatives products at Fisher Scientific. This reaction involves the bromination of a sample of either cis or trans - cinnamic acid (IUPAC name: 3-phenylpropenoic acid) to form 2,3-dibromo-3-phenylpropanoic acid. The IUPAC name of cinnamic acid is: The IUPAC name of cinnamic acid is: Skip navigation Sign in. The Cinnamic acid is an organic compound with the formula C 9 H 8 O 2. It contains a double bond at second carbon atom. It serves as a precursor to the sweetener aspartame through enzyme-catalyzed amination to phenylalanine. Cinnamic acid. Description. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. Search. Synonym: (2E)-3-Phenyl-2-propenoic acid, trans-3-Phenylacrylic acid, trans-Cinnamic acid Empirical Formula (Hill Notation): C 9 H 8 O 2 Molecular Weight: 148.16 Display Name: trans-cinnamic acid EC Number: 205-398-1 EC Name: trans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 IUPAC Name: (2E)-3-phenylprop-2-enoic acid . CHEMISTRY 2400 FALL 2020 EXPERIMENT 6: BROMINATION OF CINNAMIC ACID Text reference: Bruice sections 6.9 and 6.13 (8 th Ed.) It has a melting point of 133 degree centigrade and a boiling point of 300 degree centigrade. The parent compound is propanoic acid. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. IUPAC Name: (E)-3-phenylprop-2-enoic acid . This video is unavailable. 2.6k SHARES. Common Name: Cinnamic acid: Description: Cinnamic acid, also known as (Z)-cinnamate or 3-phenyl-acrylate, belongs to the class of organic compounds known as cinnamic acids. Cinnamic acid is an organic compound with the formula C 6 H 5 CHCHCO 2 H. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. It is found in Cinnamomum cassia. The IUPAC name of cinnamic acid is: 6.6k LIKES. trans-Cinnamic Acid: Intervalo porcentual del ensayo ≥99%: Número MDL: MFCD00004369: Índice Merck: 14,2299: Información sobre solubilidad: Soluble in many organic solvents. or 6.9 and 6.15 (7 th Ed.) trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. ChEBI Ontology Outgoing trans-cinnamic acid (CHEBI:35697) has role plant metabolite (CHEBI:76924) trans-cinnamic acid (CHEBI:35697) is a cinnamic acid (CHEBI:27386) trans-cinnamic acid (CHEBI:35697) is conjugate acid of trans-cinnamate (CHEBI:15669) Text Solution. Name: trans-Cinnamic acid. With the CAS registry number 621-82-9, it is also named as 3c-phenyl-acrylic acid. Slightly soluble in water. And it is an oily yellow liquid at room temperature with a boiling point of 246 °C. Cinnamic acid, derivatives of cinnamic acid (HCA, DHCA, MHMMCA, DMCA, MHDMCA and TMCA) were procured from Sigma Aldrich, St. Louis, MO, USA. It is involved in the production of methyl, ethyl and benzyl esters, which is used in the perfume industry. Fisher Scientific ; Fisher Healthcare ; Fisher Science Education ; Sign Up for Email NEW Help & Support Center ›+1-800-766-7000; 0. Stars This entity has been manually annotated by the ChEBI Team. General information; Classification & Labelling & PBT assessment; Manufacture, use & exposure Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. Cinnamic acid is an organic compound with the formula C6H5CH=CHCOOH. Cinnamic acid is an organic compound with the formula C6H5CHCHCO2H. Structure, properties, spectra, suppliers and links for: Cinnamic acid, phenyl ester, 2757-04-2. Loading... Close. Classified as an unsaturated carboxylic acid 2.6k VIEWS. Chemical Name or Material: trans-Cinnamic Acid: Assay Percent Range ≥99%: MDL Number: MFCD00004369: Merck Index: 14,2299: Solubility Information: Soluble in many organic solvents. The acid is used to produce flavorings, synthetic indigo, pharmaceuticals, perfumes, and aspartame sweeteners. Cinnamic acid is a white crystalline odorless organic acid. View our Cinnamic acid amides products at Fisher Scientific. Type of substance Composition: mono-constituent substance Origin: organic Total tonnage band Total range: Intermediate Use Only REACH Registered as: Structural formula of cinnamic acid => C6H5CHCHCO2H (C9H8O2). Chemical Formula: C 9 H 8 O 2. click here for details. The IUPAC name of C 6 H 5 C H = C H − C O O H is 3 - Phenyl prop - 2 - enoic acid. 2,3-dihydroxy butane dioic acid 1-pheny-2-carboxy ethane 3-phenyl prop-2-enoic acid dihydroxy-3-phenyl propionic acid Answer : C Related Video. View All. Common Name: trans-Cinnamic acid: ... Cinnamic acid has the formula C6H5CHCHCOOH and is an odorless white crystalline acid, which is slightly soluble in water. The product's classification codes are Drug / Therapeutic Agent; Skin / Eye Irritant. It has a melting point of 133 degrees and a boiling point of 300 degrees. Chemical Formula: C 9 H 8 O 2. click here for details. The IUPAC name of this chemical is (E)-3-phenylprop-2-enoic acid. Display Name: trans-cinnamic acid EC Number: 205-398-1 EC Name: trans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 IUPAC Name: (2E)-3-phenylprop-2-enoic acid . 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 … More information on the manner in which spectra in this collection were collected can be found here. Watch Queue Queue. 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