cinnamic acid formula

See more. Cynarin analytical standard provided with w/w absolute assay, to be used for quantitative titration. Chemical Formula: C 9 H 8 O 2. click here for details. Structure, properties, spectra, suppliers and links for: Cinnamic acid, 621-82-9. The chemical formula of CINNAMIC ACID shown above is based on the molecular formula indicating the numbers of each type of atom in a molecule without structural information, which is different from the empirical formula which provides the numerical proportions of atoms of each type. Soluble in 3 vols of 70% alc. α-Cyano-4-hydroxycinnamic acid; Caffeic acid – burdock, hawthorn, artichoke, pear, basil, thyme, oregano, apple Details of the supplier of the safety data sheet Emergency Telephone Number During normal business hours (Monday-Friday, 8am-7pm EST), call … These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. 140-10-3 - WBYWAXJHAXSJNI-VOTSOKGWSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. Miscible with alcohol, ether. Chemical Name (E)-3-[4-(dimethylamino)phenyl]prop-2-enoic acid: SMILES: CN(C)C1=CC=C(C=C1)C=CC(=O)O: Standard InChIKey: CQNPVMCASGWEHM-VMPITWQZSA-N: General tips: For obtaining a higher solubility , … Cinnamaldehyde, or 3-phenylprop-2-enal to use its IUPAC name, is a member of the class of compounds known as cinnamaldehydes. PubMed:Design and synthesis of conformationally constrained analogues of cis-cinnamic acid and evaluation of their plant growth inhibitory activity. cinnamaldehyde, cinnamic acid, citric acid, and levulinic acid Compound Structure Molecular Formula Molecular Weight (Da) Solubility (M) Citric acid Levulinic acid C 6 H 8 O 7 192.12 4.809 M in water Cinnamic acid C 5 H 8 O 3 116.11 6.746 M in water Cinnamaldehyde C 9 H 8 O 2 148.16 0.004 M in water C 9 H 8 O 132.16 0.008 M in water Cinnamic acid is a white crystalline compound with the formula C6H5CH=CHCOOH which is slightly soluble in water, and freely soluble in many organic solvents. IUPAC Name: (E)-3-phenylprop-2-enoic acid . SCHEMBL18229947. Sinapic acid. Cinnamic acid deriv. mp 6-10°. Formula : C₂₁H₂₀O₆ ; MSDS (6) - Specification (1) MSDS (6) Español; Français; English; Italian; Portuguese; German; Specification (1) English; 88.00 € Détails and order. Cinnamic acid was used in this lab because as a naturally occurring compound, it has many different uses. Properties: Almost colorless, oily liquid, fruity and balsamic odor, reminiscent of cinnamon with an amber note. Sinapic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration. Formula: C11H13NO2: M.Wt: 191.23: Type of Compound: Alkaloids: Storage: Desiccate at -20°C Solubility: Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. Cinnamic acids play key roles in the formation of other more complex phenolic compounds. 16 / 106. It is also used in some perfumes of natural, sweet, or fruity scents. chemBlink provides information about CAS # 140-10-3, trans-Cinnamic acid, 3-Phenyl-2-propenoic acid, trans-3-Phenylacrylic acid, molecular formula: C9H8O2. It is found in Cinnamomum cassia. 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 trans-Cinnamic acid, also known as (e)-cinnamic acid or phenylacrylic acid, belongs to the class of organic compounds known as cinnamic acids. : A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid; trans-3-Phenylacrylic acid Recommended Use Laboratory chemicals. Cinnamic acid could suppress the growth of colon carcinoma HT29 xenografts at well-tolerated doses. 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. Stars This entity has been manually annotated by the ChEBI Team. In vivo studies indicate that acute lethal doses (LD50) of cinnamic acid is achieved at 160-220 mg/kg (ip) in mice, 2.5 g/kg (oral) in rats and 5 g/kg (dermal) in rabbits. 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. trans-Cinnamic acid exists in all living species, ranging … Uses advised against Food, drug, pesticide or biocidal product use. Also, several hydroxycinnamic acid derivatives, such as cinnamic acid, ameliorated the obesity induced by an HFD in rats [106]. trans-Cinnamic-d7 acid. The most obvious application for cinnamaldehyde is as flavoring in chewing gum, ice cream, candy, eliquid and beverages; use levels range from 9 to 4,900 parts per million (that is, less than 0.5%). Insol in water. The measurement of the melting point allows determining the addition mode of the bromine to the double bond. d 2525 1.045-1.048. d 420 1.049. bp 271°. 4501-31-9 - NGSWKAQJJWESNS-UTCJRWHESA-N - Cinnamic acid, p-hydroxy-, (Z)- - Similar structures search, synonyms, formulas, resource links, and other chemical information. Cinnamic acid and harpagoside are important active components present in Scrophularia ningpoensis, which has been used in the treatment of several diseases such as pharyngalgia. These compounds are hydroxy derivatives of cinnamic acid.. Articles of trans-Cinnamic acid are included as well. trans-CINNAMIC ACID, POTASSIUM SALT cinnamic acid, sodium salt phenylhydrazine, cinnamate(1:1) Cinnamic acid, ethyl ester trans-CINNAMIC ACID, ETHYL ESTER VINYL CINNAMATE Cinnamoyl chloride 3-PHENYL-ACRYLOYL-CHLORIDE KCMITHMNVLRGJU-CMDGGOBGSA-N Cinnamic acid allyl ester Cinnamic acid deriv. 5 / 14. It is used as a flavoring, in perfumes, and is a source to a large number of other natural substances. NEW. n D20 1.559-1.561. Autoxidation produces cinnamic acid. TLC and 1H NMR analysis confirm the purity of final product, without any cinnamic acid contamination, and thus it is not necessary to make any recrystallization. Google Patents:Cis-cinnamic acid anti-inflammatory compositions and process of treating inflammation and capillary fragility PubMed:cis-Cinnamic acid selective suppressors distinct from auxin inhibitors. Hydroxycinnamic acids (hydroxycinnamates) are a class of aromatic acids or phenylpropanoids having a C 6 –C 3 skeleton. Resources Search for: CINNAMIC ACID . trans-Cinnamic-d7 acid, 98 atom % D Synonym: 3,5-Dimethoxy-4-hydroxycinnamic acid, 4-Hydroxy-3,5-dimethoxy-cinnamic acid, Sinapinic acid Empirical Formula (Hill Notation): C 11 H 12 O 5 Molecular Weight: 224.21 DTXSID50584103. The percentage yield of the Cinnamic acid is about 64.8% of melting point 132 °C. 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