CAS 945-93-7
:ethyl trans-beta-methylcinnamate
Description:
Ethyl trans-beta-methylcinnamate is an organic compound classified as an ester, specifically derived from cinnamic acid and ethanol. It features a trans configuration around the double bond, which contributes to its unique structural and sensory properties. The compound is characterized by its pleasant, sweet, and floral aroma, making it a popular choice in the fragrance and flavor industries. Ethyl trans-beta-methylcinnamate is typically a colorless to pale yellow liquid with a moderate boiling point and low solubility in water, but it is soluble in organic solvents. Its molecular structure includes a phenyl ring, a double bond, and an ethyl ester functional group, which influence its reactivity and stability. This compound is often used in perfumes, cosmetics, and food flavorings due to its aromatic qualities. Additionally, it may exhibit some biological activity, although specific studies on its pharmacological effects are limited. As with many organic compounds, proper handling and safety measures should be observed due to potential irritant properties.
Formula:C12H14O2
Synonyms:- ETHYL TRANS-BETA-METHYLCINNAMATE
- Cinnamic acid, .beta.-methyl-, ethyl ester
- Ethyl 3-phenylcrotonate
- Ethylbeta-methylcinnamate
- Nsc20769
- ETHYL B-METHYLCINNAMATE
- 2-Butenoic acid, 3-phenyl-, ethyl ester
- 2-BUTENOIC ACID, 3-PHENYL-ETHYL ESTER(E)
- Ethyl 3-phenyl-2- butenoate
- ETHYLTRANS-β-METHYLCINNAMATE
- ethyl (E)-3-phenylbut-2-enoate
- ETHYL TRANS-BETA-METHYLCINNAMATE USP/EP/BP
- 3-Phenyl-but-2-enoic acid ethyl ester
- Ethyl 3-phenylbut-2-enoate (E/Z mixture)
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Ethyl 3-phenylbut-2-enoate (E/Z mixture)
CAS:Formula:C12H14O2Purity:98%Color and Shape:LiquidMolecular weight:190.2384Ethyl 3-Phenylbut-2-enoate
CAS:Formula:C12H14O2Purity:98%Color and Shape:Solid, No data available.Molecular weight:190.242Ethyl 3-phenylbut-2-enoate
CAS:<p>Ethyl 3-phenylbut-2-enoate is an ancillary for the production of styrene, ring-opening, bond cleavage of aldehydes and epoxides, and activation of olefinic compounds. It has been used to make advances in the stereochemistry of ethyl diazoacetate and other nature products. The compound is also used as an intermediate in the synthesis of isomeric ethyl 3-(phenylpropionate)acrylate.</p>Formula:C12H14O2Purity:Min. 95%Molecular weight:190.24 g/mol


