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CAS 78543-08-5

:

1,3-Diethyl 2-(4-amino-3-fluorophenyl)-2-methylpropanedioate

Description:
1,3-Diethyl 2-(4-amino-3-fluorophenyl)-2-methylpropanedioate, identified by its CAS number 78543-08-5, is an organic compound characterized by its complex structure, which includes an ester functional group and an amino group. This compound features a diethyl ester moiety, indicating the presence of two ethyl groups attached to the carboxylic acid part of the molecule. The presence of a 4-amino-3-fluorophenyl group suggests that it has both amino and fluorine substituents on the aromatic ring, which can influence its reactivity and biological activity. The methylpropanedioate backbone contributes to its overall stability and solubility properties. Typically, compounds of this nature may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. Additionally, the presence of fluorine can enhance lipophilicity and metabolic stability. Overall, this compound's unique structural features may lead to diverse applications in pharmaceuticals or agrochemicals, although specific applications would depend on further research and characterization.
Formula:C14H18FNO4
InChI:InChI=1S/C14H18FNO4/c1-4-19-12(17)14(3,13(18)20-5-2)9-6-7-11(16)10(15)8-9/h6-8H,4-5,16H2,1-3H3
InChI key:InChIKey=AXSSLCGWLSGEET-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)(C(OCC)=O)(C)C1=CC(F)=C(N)C=C1
Synonyms:
  • 1,3-Diethyl 2-(4-amino-3-fluorophenyl)-2-methylpropanedioate
  • 2-(4-Amino-3-fluorophenyl)-2-methylmalonic acid diethyl ester
  • Diethyl (4-Amino-3-Fluorobenzyl)Propanedioate
  • Diethyl 2-(4-amino-3-fluorophenyl)-2-methylpropanedioate
  • Diethyl-2-(4-amino-3-fluorophenyl)-2-methylmalonate
  • Propanedioic acid, (4-amino-3-fluorophenyl)methyl-, diethyl ester
  • Propanedioic acid, 2-(4-amino-3-fluorophenyl)-2-methyl-, 1,3-diethyl ester
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