
CAS 5048-82-8: ethyl 4-Aminocinnamate
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
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Found 3 products.
Ethyl 4-aminocinnamate
CAS: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:C11H13NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:191.23 g/molTrans-3-(4-Aminophenyl)acrylate ethyl ester
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:191.22999572753906Ethyl 3-(4-aminophenyl)acrylate
CAS:Formula:C11H13NO2Purity:98%Color and Shape:SolidMolecular weight:191.2264