Cinnamic Acid
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trans-Cinnamic acid, 99+%
CAS: 140-10-3 Molecular Formula: C9H8O2 Molecular Weight (g/mol): 148.161 MDL Number: MFCD00004369 InChI Key: WBYWAXJHAXSJNI-VOTSOKGWSA-N Synonym: cinnamic acid,trans-cinnamic acid,e-cinnamic acid,3-phenylacrylic acid,trans-3-phenylacrylic acid,zimtsaeure,2e-3-phenylprop-2-enoic acid,3-phenylprop-2-enoic acid,3-phenylpropenoic acid PubChem CID: 444539 ChEBI: CHEBI:35697 IUPAC Name: (E)-3-phenylprop-2-enoic acid SMILES: C1=CC=C(C=C1)C=CC(=O)O
| PubChem CID | 444539 |
|---|---|
| CAS | 140-10-3 |
| Molecular Weight (g/mol) | 148.161 |
| ChEBI | CHEBI:35697 |
| MDL Number | MFCD00004369 |
| SMILES | C1=CC=C(C=C1)C=CC(=O)O |
| Synonym | cinnamic acid,trans-cinnamic acid,e-cinnamic acid,3-phenylacrylic acid,trans-3-phenylacrylic acid,zimtsaeure,2e-3-phenylprop-2-enoic acid,3-phenylprop-2-enoic acid,3-phenylpropenoic acid |
| IUPAC Name | (E)-3-phenylprop-2-enoic acid |
| InChI Key | WBYWAXJHAXSJNI-VOTSOKGWSA-N |
| Molecular Formula | C9H8O2 |
trans-Cinnamic Acid, 98+%
CAS: 140-10-3 Molecular Formula: C9H8O2 Molecular Weight (g/mol): 148.161 MDL Number: MFCD00004369 InChI Key: WBYWAXJHAXSJNI-VOTSOKGWSA-N Synonym: cinnamic acid,trans-cinnamic acid,e-cinnamic acid,3-phenylacrylic acid,trans-3-phenylacrylic acid,zimtsaeure,2e-3-phenylprop-2-enoic acid,3-phenylprop-2-enoic acid,3-phenylpropenoic acid PubChem CID: 444539 ChEBI: CHEBI:35697 IUPAC Name: (E)-3-phenylprop-2-enoic acid SMILES: C1=CC=C(C=C1)C=CC(=O)O
| PubChem CID | 444539 |
|---|---|
| CAS | 140-10-3 |
| Molecular Weight (g/mol) | 148.161 |
| ChEBI | CHEBI:35697 |
| MDL Number | MFCD00004369 |
| SMILES | C1=CC=C(C=C1)C=CC(=O)O |
| Synonym | cinnamic acid,trans-cinnamic acid,e-cinnamic acid,3-phenylacrylic acid,trans-3-phenylacrylic acid,zimtsaeure,2e-3-phenylprop-2-enoic acid,3-phenylprop-2-enoic acid,3-phenylpropenoic acid |
| IUPAC Name | (E)-3-phenylprop-2-enoic acid |
| InChI Key | WBYWAXJHAXSJNI-VOTSOKGWSA-N |
| Molecular Formula | C9H8O2 |
Sigma Aldrich trans-Cinnamic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Boiling Point | 300°C (lit.) |
|---|---|
| Percent Purity | ≥99% |
| Linear Formula | C6H5CH=CHCOOH |
| CAS | 140-10-3 |
| Molecular Weight (g/mol) | 148.16 |
| MDL Number | MFCD00004369 |
| Synonym | trans-3-Phenylacrylic acid; Cinnamic acid |
| RTECS Number | GD7850000 |
| Recommended Storage | Room Temperature |
| Molecular Formula | C9H8O2 |
| EINECS Number | 205-398-1 |
| Melting Point | 132°C to 135°C (lit.) |
Sigma Aldrich Fine Chemicals Biosciences trans Cinnamic acid natura1KG
trans-Cinnamic acid is an -unsaturated aromatic acid that can be used as a flavoring agent. It is mainly used to prepare ester derivatives that are used in perfume industry. trans-Cinnamic acid is the key volatile components of cinnamon essential oil.
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Sigma Aldrich Fine Chemicals Biosciences Cinnamic acid United States Pharmacopeia (USP) Reference Standard | 140-10-3 | MFCD00004369 | 100MG
Cinnamic acid United States Pharmacopeia (USP) Reference Standard | Mol Wt: 148.16 | 140-10-3 | MFCD00004369 | 100MG
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Selleck Chemical LLC Cinnamic acid S3677-25mg
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Cinnamic acid (Benzenepropenoic acid Isocinnamic acid trans-Cinnamic acid Phenylacrylic acid) a naturally occurring aromatic fatty acid of low toxicity induces cytostasis and a reversal of malignant properties of human tumor cells in vitro
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Selleck Chemical LLC Cinnamic acid S3677-1g
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Cinnamic acid (Benzenepropenoic acid Isocinnamic acid trans-Cinnamic acid Phenylacrylic acid) a naturally occurring aromatic fatty acid of low toxicity induces cytostasis and a reversal of malignant properties of human tumor cells in vitro
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Alkali Scientific Trans Cinnamic Acid [B Phenylacrylic acid], 100 G
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Trans Cinnamic Acid (Phenylacrylic Acid) is a chemical compound widely used as a laboratory reagent. This powder form of trans cinnamic acid, a key aromatic compound, is crucial in various research areas such as organic synthesis, molecular biology, and pharmaceutical development. It is commonly used for studying the properties and reactions of phenylacrylic acid derivatives, which play a significant role in the formation of bioactive compounds. Researchers use this reagent in the synthesis of flavonoids, phenolic compounds, and other bioactive molecules. Its applications extend into pharmacology, cosmetics, and agriculture, especially in studies related to plant metabolism and anti-inflammatory properties.
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