CAS 5396-71-4
:2-Propenoic acid, 3-(3-nitrophenyl)-, ethyl ester
Description:
2-Propenoic acid, 3-(3-nitrophenyl)-, ethyl ester, commonly known as ethyl 3-(3-nitrophenyl)acrylate, is an organic compound characterized by its acrylate structure, which features a vinyl group and an ester functional group. This compound typically appears as a yellow to amber liquid and is known for its reactivity, particularly in polymerization processes due to the presence of the double bond in the propenoic acid moiety. The nitrophenyl group contributes to its electronic properties, potentially enhancing its reactivity in electrophilic aromatic substitution reactions. It is soluble in organic solvents and may exhibit moderate stability under standard conditions, although it can be sensitive to light and heat. The compound is of interest in various applications, including as a building block in organic synthesis and in the production of polymers and copolymers. Safety precautions should be taken when handling this substance, as it may pose health risks, including irritation to the skin and eyes, and potential toxicity if ingested or inhaled.
Formula:C11H11NO4
InChI:InChI=1S/C11H11NO4/c1-2-16-11(13)7-6-9-4-3-5-10(8-9)12(14)15/h3-8H,2H2,1H3
InChI key:InChIKey=QZEPRSLOWNHADS-UHFFFAOYSA-N
SMILES:C(=CC(OCC)=O)C1=CC(N(=O)=O)=CC=C1
Synonyms:- 2-Propenoic acid, 3-(3-nitrophenyl)-, ethyl ester
- 2-{[2-Chloro-5-(Morpholin-4-Ylsulfonyl)Phenyl]Amino}-2-Oxoethyl Pyrazine-2-Carboxylate
- 3-(3-Nitrophenyl)-2-propenoic acid ethyl ester
- 3-(3-Nitrophenyl)acrylic acid ethyl ester
- 3-Nitrocinnamic acid ethyl ester
- Cinnamic acid, m-nitro-, ethyl ester
- Ethyl m-nitrocinnamate
- NSC 4346
- ethyl (2E)-3-(3-nitrophenyl)prop-2-enoate
- Ethyl 3-nitrocinnamate
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Found 5 products.
Ethyl 3-(3-Nitrophenyl)Acrylate
CAS:<p>Ethyl 3-(3-Nitrophenyl)Acrylate</p>Purity:98%Molecular weight:221.21g/molEthyl 3-nitrocinnamate
CAS:<p>Ethyl 3-nitrocinnamate is a synthetic compound that belongs to the group of stilbene derivatives. It has been used as an intermediate in the synthesis of other compounds. Ethyl 3-nitrocinnamate is not naturally occurring and can be synthesized by isomerization of cinnamic acid and nitration of ethyl cinnamate. The stereochemical and stereoselective properties of this compound can be utilized for the synthesis of other compounds. Nitrobenzaldehyde reacts with nitrovinyl chloride to form oxetane, which then reacts with acetonitrile to produce ethyl 3-nitrocinnamate.</p>Formula:C11H11NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:221.21 g/mol



