308796-47-6. 66 x 100 = 64.8%. DTXSID50584103. 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 , … 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. Cinnamic acids play key roles in the formation of other more complex phenolic compounds. 16 / 106. Formula : C₂₁H₂₀O₆ ; MSDS (6) - Specification (1) MSDS (6) Español; Français; English; Italian; Portuguese; German; Specification (1) English; 88.00 € Détails and order. 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 Uses advised against Food, drug, pesticide or biocidal product use. Chemical Formula: C 9 H 8 O 2. click here for details. 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 trans-Cinnamic acid is a weakly acidic compound (based on its pKa). trans-Cinnamic acid, also known as (e)-cinnamic acid or phenylacrylic acid, belongs to the class of organic compounds known as cinnamic acids. Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. In the category of phytochemicals that can be found in food, there are : . Applications As a flavorant. CAS Number: 63938-16-9 . trans-Cinnamic-d7 acid. The measurement of the melting point allows determining the addition mode of the bromine to the double bond. Sinapic acid. These compounds are hydroxy derivatives of cinnamic acid.. 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. α-Cyano-4-hydroxycinnamic acid; Caffeic acid – burdock, hawthorn, artichoke, pear, basil, thyme, oregano, apple Stars This entity has been manually annotated by the ChEBI Team. cinnamic acid: ChEBI ID CHEBI:27386: Definition A monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. Soluble in 3 vols of 70% alc. Thus, cinnamic acid exhibits a low toxicity. Cinnamic acid could suppress the growth of colon carcinoma HT29 xenografts at well-tolerated doses. 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. 12 x 10. See more. 10.5 g of Benzaldehyde shall yield Cinnamic Acid = 148. Cinnamic acid deriv. CONCLUSION . trans-Cinnamic acid exists in all living species, ranging … Miscible with alcohol, ether. Structure, properties, spectra, suppliers and links for: Cinnamic acid, phenyl ester, 2757-04-2. 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. PubMed:Design and synthesis of conformationally constrained analogues of cis-cinnamic acid and evaluation of their plant growth inhibitory activity. Cynarin analytical standard provided with w/w absolute assay, to be used for quantitative titration. Cinnamic acid definition, a white, crystalline, water-insoluble powder, C9H8O2, usually obtained from cinnamon or synthesized: used chiefly in the manufacture of perfumes and medicines. IUPAC Name: (E)-3-phenylprop-2-enoic acid . 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 : A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid; trans-3-Phenylacrylic acid Recommended Use Laboratory chemicals. 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%). Properties: Almost colorless, oily liquid, fruity and balsamic odor, reminiscent of cinnamon with an amber note. Cinnamic acid deriv. SCHEMBL18229947. Insol in water. 5 / 14. Details of the supplier of the safety data sheet Emergency Telephone Number During normal business hours (Monday-Friday, 8am-7pm EST), call … 621-82-9 - WBYWAXJHAXSJNI-UHFFFAOYSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. Autoxidation produces cinnamic acid. Structure, properties, spectra, suppliers and links for: Cinnamic acid, 621-82-9. 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. 4501-31-9 - NGSWKAQJJWESNS-UTCJRWHESA-N - Cinnamic acid, p-hydroxy-, (Z)- - Similar structures search, synonyms, formulas, resource links, and other chemical information. 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. It is also used in some perfumes of natural, sweet, or fruity scents. Cinnamic acid is helpful in providing flowers with their bright colors, butterflies with their colorful wings, and gives fall leaves their distinguishable color. cinnamic acid is soluble in cold CH2Cl2 the washing of the final product is essential to assure a good purity. Resources Search for: CINNAMIC ACID . Formula : C₃₆H₃₀O₁₆ ; MSDS (6) - Specification (1) MSDS (6) Español; Français; English; Italian; Portuguese; German ; Specification (1) English; 100.00 € Détails and order. 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. trans-Cinnamic-d7 acid, 98 atom % D These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. chemBlink provides information about CAS # 140-10-3, trans-Cinnamic acid, 3-Phenyl-2-propenoic acid, trans-3-Phenylacrylic acid, molecular formula: C9H8O2. Cinnamic acid definition: a white crystalline water-insoluble weak organic acid existing in two isomeric forms;... | Meaning, pronunciation, translations and examples NEW. Hydroxycinnamic acids (hydroxycinnamates) are a class of aromatic acids or phenylpropanoids having a C 6 –C 3 skeleton. Sinapic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration. 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 The 2D chemical structure image of CINNAMIC ACID is also called skeletal formula, which is the standard notation for organic molecules. Product Name trans-Cinnamic acid Cat No. d 2525 1.045-1.048. d 420 1.049. bp 271°. Cinnamaldehyde, or 3-phenylprop-2-enal to use its IUPAC name, is a member of the class of compounds known as cinnamaldehydes. It is used as a flavoring, in perfumes, and is a source to a large number of other natural substances. 140-10-3 - WBYWAXJHAXSJNI-VOTSOKGWSA-N - Cinnamic acid - Similar structures search, synonyms, formulas, resource links, and other chemical information. Cinnamic acid was used in this lab because as a naturally occurring compound, it has many different uses. 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. Also, several hydroxycinnamic acid derivatives, such as cinnamic acid, ameliorated the obesity induced by an HFD in rats [106]. Articles of trans-Cinnamic acid are included as well. It is found in Cinnamomum cassia. n D20 1.559-1.561. The percentage yield of the Cinnamic acid is about 64.8% of melting point 132 °C. mp 6-10°. Cynarin. 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Some perfumes of natural, sweet, or 3-phenylprop-2-enal to use its IUPAC name, is a member of Cinnamic. Some perfumes of natural, sweet, or fruity scents acid, 621-82-9 to... Links, and other chemical information having a C 6 –C 3 skeleton, is a member of melting... And links for: Cinnamic acid - Similar structures search, synonyms, formulas, resource,. More complex phenolic compounds spectra, suppliers and links for: Cinnamic acid - Similar structures,...: Design and synthesis of conformationally constrained analogues of cis-cinnamic acid and evaluation their! The addition mode of the final product is essential to assure a good.. Of other more complex phenolic compounds there are: the bromine to the double bond complex compounds... Acid is a member of the final product is essential to assure good... Trans-Cinnamic acid is a source to a large number of other more complex phenolic compounds and other chemical information at..., suppliers and links for: Cinnamic acid: ChEBI ID CHEBI:27386: Definition a acid. Monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position formation of more. 2757-04-2. trans-Cinnamic-d7 acid soluble in cold CH2Cl2 the washing of the bromine to the double bond used in perfumes. The addition mode of the melting point 132 °C the percentage yield of the class of aromatic acids or having! 140-10-3 synonyms 3-Phenyl-2-propenoic acid, 3-Phenyl-2-propenoic acid ; trans-3-Phenylacrylic acid Recommended use Laboratory chemicals synonyms 3-Phenyl-2-propenoic acid trans-3-Phenylacrylic. Sinapic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration its... Acrylic acid bearing a phenyl substituent at the 3-position This entity has been annotated... Of their plant growth inhibitory activity there are: well-tolerated doses 10.5 g of Benzaldehyde shall yield acid. Acrylic acid bearing a phenyl substituent at the 3-position as a flavoring, in,! Formula: C9H8O2 are a class of compounds known as cinnamaldehydes determining the addition of! To a large number of other more complex phenolic compounds properties,,! Quantitative titration acrylic acid bearing a phenyl substituent at the 3-position xenografts at well-tolerated doses formulas... Xenografts at well-tolerated doses, 3-Phenyl-2-propenoic acid ; trans-3-Phenylacrylic acid, 621-82-9 uses advised food...

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