CAS 5048-82-8

ethyl 4-Aminocinnamate

Description:

Ethyl 4-aminocinnamate, with the CAS number 5048-82-8, is an organic compound characterized by its structure, which includes an ethyl ester group and an amino group attached to a cinnamate backbone. This compound typically appears as a solid or crystalline substance and is known for its potential applications in pharmaceuticals and as a chemical intermediate. Ethyl 4-aminocinnamate exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many esters. Its molecular structure allows for various chemical reactions, including esterification and amination, making it a versatile compound in synthetic organic chemistry. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken. Overall, ethyl 4-aminocinnamate is a compound of interest in both academic research and industrial applications.

Formula: C₁₁H₁₃NO₂

InChI: InChI=1S/C11H13NO2/c1-2-14-11(13)8-5-9-3-6-10(12)7-4-9/h3-8H,2,12H2,1H3

InChI key: InChIKey=NRPMBSHHBFFYBF-UHFFFAOYSA-N

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

Synonyms:

• (4-(2-(Ethoxycarbonyl)ethenyl)phenyl)amine
• 2-Propenoic acid, 3-(4-aminophenyl)-, ethyl ester
• 3-(4-Aminophenyl)acrylic acid ethyl ester
• 4-Aminocinnamic acid ethyl ester
• Cinnamic acid, p-amino-, ethyl ester
• Ethyl 4-aminocinnamate, (4-Aminocinnamic acid ethyl ester)
• Ethyl 3-(4-aminophenyl)-2-propenoate
• Ethyl 3-(4-aminophenyl)acrylate
• Ethyl p-aminocinnamate
• NSC 44439
• ethyl (2E)-3-(4-aminophenyl)prop-2-enoate

Ethyl 3-(4-aminophenyl)acrylate

CAS: 5048-82-8

Formula: C₁₁H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 191.2264

Ref: IN-DA0034V5

Ethyl 4-aminocinnamate

CAS: 5048-82-8

Ethyl 4-aminocinnamate is a supramolecular, homologous, activated, linear polymer. It is used as an amine and phosphazene ligand in mesomorphic solid-state chemistry. It has a reversible covalent bond that can be thermally broken and re-formed. This property allows for the synthesis of polymers with functional groups on both ends of the molecule. The nitro group on this compound can be reduced to amine to give another functional group. Ethyl 4-aminocinnamate has been shown to have pharmacokinetic properties that are similar to those of ethyl 4-aminobenzoate (EB). EB is an inhibitor of NS5B polymerase that blocks RNA synthesis and leads to inhibition of viral replication. EB also inhibits ring opening reactions in the presence of nitro groups, which may explain its inhibitory effect on HIV RNA synthesis.

Formula: C₁₁H₁₃NO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 191.23 g/mol

Ref: 3D-FE37168

trans-3-(4-Aminophenyl)acrylate ethyl ester

CAS: 5048-82-8

Formula: C₁₁H₁₃NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 191.23

Ref: 10-F040449