CAS 4407-36-7
:trans-Cinnamyl alcohol
Description:
Trans-cinnamyl alcohol is an organic compound characterized by its aromatic structure and is classified as a phenylpropanoid. It is a colorless to pale yellow liquid with a sweet, floral aroma reminiscent of cinnamon, which contributes to its use in the fragrance and flavor industries. The compound has a molecular formula of C9H10O and features a trans configuration around the double bond between the carbon atoms, which influences its physical properties and reactivity. Trans-cinnamyl alcohol is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. It exhibits moderate volatility and can undergo various chemical reactions, including oxidation and esterification. Additionally, trans-cinnamyl alcohol has been studied for its potential biological activities, including antimicrobial and anti-inflammatory properties. Its CAS number, 4407-36-7, is used for identification in chemical databases and regulatory contexts. Overall, trans-cinnamyl alcohol is valued for its sensory attributes and potential applications in various fields, including cosmetics and pharmaceuticals.
Formula:C9H10O
InChI:InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+
InChI key:InChIKey=OOCCDEMITAIZTP-QPJJXVBHSA-N
SMILES:C(=C/CO)\C1=CC=CC=C1
Synonyms:- trans-Cinnamyl alcohol
- 2-Propen-1-ol, 3-phenyl-, (E)-
- (2E)-3-Phenyl-2-propen-1-ol
- 2-Propen-1-ol, 3-phenyl-, (2E)-
- Cinnamyl alcohol, (E)-
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Found 8 products.
(E)-Cinnamyl Alcohol
CAS:Formula:C9H10OPurity:>97.0%(GC)Color and Shape:White or Colorless to Light yellow powder to lump to clear liquidMolecular weight:134.183-Phenyl-2-propen-1-ol
CAS:The compounds 3-phenyl-2-propen-1-ol , 2-methyl-3-butyn-2-ol, 3,7-dimethylnonane, and 2-hydroxybenzoic acid occurred only during estrus which may be consideredFormula:C9H10OColor and Shape:SolidMolecular weight:134.183-Phenyl-2-propen-1-ol
CAS:<p>3-Phenyl-2-propen-1-ol is a cinnamyl compound that is found in plants, such as cinnamon and cassia. It has been shown to have an inhibitory effect on the enzyme activities of sorbitol dehydrogenase, which is involved in the synthesis of polysaccharides. 3-Phenyl-2-propen-1-ol also has a transcriptional regulatory effect on genes that encode enzymes involved in the synthesis of polymers. The reaction mechanism for this reaction has been proposed to be through an initial nucleophilic attack by the hydroxyl group on the electrophilic carbonyl carbon atom followed by protonation and elimination of water. <br>3-Phenyl-2-propen-1-ol has also been shown to be a signal peptide, which is used to identify proteins for transport within cells. This polymerase chain reaction (PCR) model system can be used to determine</p>Formula:C9H10OPurity:Min. 95%Color and Shape:PowderMolecular weight:134.18 g/mol







