CAS 953-26-4

Ethyl 4-nitrocinnamate

Description:

Ethyl 4-nitrocinnamate is an organic compound characterized by its ester functional group and a nitro substituent on the aromatic ring. It is derived from cinnamic acid, where the hydrogen of the carboxylic acid is replaced by an ethyl group, and a nitro group is attached to the para position of the aromatic ring. This compound typically appears as a yellow to orange crystalline solid and is known for its moderate solubility in organic solvents. Ethyl 4-nitrocinnamate exhibits interesting chemical properties, including the potential for undergoing various reactions such as nucleophilic substitution and reduction due to the presence of the nitro group. It is often utilized in organic synthesis and may serve as an intermediate in the production of other chemical compounds. Additionally, its derivatives can be explored for applications in pharmaceuticals and agrochemicals. Safety data should be consulted, as nitro compounds can be hazardous, and appropriate handling procedures should be followed.

Formula: C₁₁H₁₁NO₄

InChI: InChI=1S/C11H11NO4/c1-2-16-11(13)8-5-9-3-6-10(7-4-9)12(14)15/h3-8H,2H2,1H3

InChI key: InChIKey=PFBQVGXIMLXCQB-UHFFFAOYSA-N

SMILES: C(=CC(OCC)=O)C1=CC=C(N(=O)=O)C=C1

Synonyms:

• 2-Propenoic acid, 3-(4-nitrophenyl)-, ethyl ester
• 3-(4-Nitrophenyl)-2-propenoic acid ethyl ester
• 3-(4-Nitrophenyl)acrylic acid ethyl ester
• 4-Nitrocinnamic acid ethyl ester
• 4-Nitrocinnamicacidethylester
• Cinnamic acid, p-nitro-, ethyl ester
• Ethyl 3-(4-Nitrophenyl)Prop-2-Enoate
• Ethyl 3-(4-nitrophenyl)-2-propenoate
• Ethyl 4-nitrocinnamate,predominantly trans
• Ethyl p-nitrocinnamate
• Ethyl4-nitrocinnamate
• Ethyl4-nitrocinnnamate
• NSC 4697
• NSC 636709
• ethyl (2E)-3-(4-nitrophenyl)prop-2-enoate
• ethyl (2Z)-3-(4-nitrophenyl)prop-2-enoate
• Ethyl 4-nitrocinnamate
• Ethyl 4-nitrocinnamate
• ETHYL 4-NITROCINNNAMATE
• Ethyl (2E)-3-(4-nitrophenyl)-2-propenoate
• 4-Nitrobenzeneacrylic acid ethyl ester
• ETHYL 4-NITROCINNAMATE, 99%, PREDOMINANT LY TRANS
• AKOS 344
• 4-Nitrozimtsaeure-ethylester
• 3-(4-Nitrophenyl)propenoic acid ethyl ester
• Ethyl 4-nitrocinnamate, predominantly trans, 99%
• 3-(4-nitrophenyl)-2-propenoicaciethylester
• Propenoic acid, 3-(4-nitrophenyl)-, ethyl ester
• p-nitro-cinnamicaciethylester

Ethyl 4-nitrocinnamate

CAS: 953-26-4

Ethyl 4-nitrocinnamate

Formula: C₁₁H₁₁NO₄

Purity: 95%

Molecular weight: 221.20934

Ref: 54-OR480578

Ethyl 4-Nitrocinnamate

CAS: 953-26-4

Formula: C₁₁H₁₁NO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 221.2093

Ref: IN-DA003QBI

Ethyl 4-nitrocinnamate

CAS: 953-26-4

Ethyl 4-nitrocinnamate

Formula: C₁₁H₁₁NO₄

Purity: 95% (E)

Molecular weight: 221.21

Ref: IN-DG23242

Ethyl 4-nitrocinnamate

CAS: 953-26-4

Formula: C₁₁H₁₁NO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 221.212

Ref: 10-F002995

Ethyl 4-nitrocinnamate

CAS: 953-26-4

Ethyl 4-nitrocinnamate is an organic compound that is a white solid. It is soluble in water and has a density of 1.12 g/cm3. Ethyl 4-nitrocinnamate has been used as a ligand for coordination complexes with a variety of metal ions, including alkali metals, such as sodium and potassium. The reaction rate of ethyl 4-nitrocinnamate with diazoacetate is slow, but the rate increases when chloride ion is added to the reaction solution. The addition of nitrovinyl chloride to the reaction solution causes an increase in the reaction rate. This may be due to its ability to stabilize the ethyl cinnamate intermediate formed during the first step of the reaction process.

Formula: C₁₁H₁₁NO₄

Purity: Min. 95%

Molecular weight: 221.21 g/mol

Ref: 3D-FE34419